Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv6019607

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:62

Publication(s):Wu et al. 2021

Links to Other Resources

Overlapping Genes

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: 131 SVs from 31 studies. See in: genome view

Submitted genomic111,641,913-111,641,974

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6019607	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	111,641,913	111,641,974
nsv6019607	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	114,404,193	114,404,254

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17584596	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17584596	Submitted genomic		NC_000009.12:g.111 641913_111641974de l	GRCh38 (hg38)		NC_000009.12	Chr9	111,641,913	111,641,974
nssv17584596	Remapped	Perfect	NC_000009.11:g.114 404193_114404254de l	GRCh37.p13	First Pass	NC_000009.11	Chr9	114,404,193	114,404,254

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

You are here: NCBI