nsv7139144
- Organism: Homo sapiens
- Study:nstd232 (Keane et al. 2023)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:54
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 1065 SVs from 77 studies. See in: genome view
Overlapping variant regions from other studies: 605 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 605 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 1065 SVs from 77 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv7139144 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 241,985,514 | 241,985,567 |
| nsv7139144 | Remapped | Perfect | GRCh38.p12 | ALT_REF_LOCI_1 | Second Pass | NT_187523.1 | Chr2|NT_18 7523.1 | 24,209 | 24,262 |
| nsv7139144 | Remapped | Perfect | GRCh38.p12 | ALT_REF_LOCI_2 | Second Pass | NT_187647.1 | Chr2|NT_18 7647.1 | 24,209 | 24,262 |
| nsv7139144 | Submitted genomic | GRCh37.p13 | Primary Assembly | NC_000002.11 | Chr2 | 242,927,665 | 242,927,718 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv18832934 | deletion | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv18832934 | Remapped | Perfect | NT_187523.1:g.2420 9_24262del | GRCh38.p12 | Second Pass | NT_187523.1 | Chr2|NT_18 7523.1 | 24,209 | 24,262 |
| nssv18832934 | Remapped | Perfect | NT_187647.1:g.2420 9_24262del | GRCh38.p12 | Second Pass | NT_187647.1 | Chr2|NT_18 7647.1 | 24,209 | 24,262 |
| nssv18832934 | Remapped | Perfect | NC_000002.12:g.241 985514_241985567de l | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 241,985,514 | 241,985,567 |
| nssv18832934 | Submitted genomic | NC_000002.11:g.242 927665_242927718de l | GRCh37.p13 | NC_000002.11 | Chr2 | 242,927,665 | 242,927,718 |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Genotype Information
| Variant Call ID | Allele Frequency (AF) | Allele Count (AC) | Allele Number (AN) |
|---|---|---|---|
| nssv18832934 | 0.5 | 1 | 2 |