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dbVar

Database of genomic structural variation

nsv6043082

Organism: Homo sapiens

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

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

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: 126 SVs from 27 studies. See in: genome view

Submitted genomic64,989,255-64,989,255

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6043082	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	64,989,255	64,989,255
nsv6043082	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	65,216,389	65,216,389

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17522150	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17522150	Submitted genomic		NC_000002.12:g.649 89255_64989256ins9 5	GRCh38 (hg38)		NC_000002.12	Chr2	64,989,255	64,989,255
nssv17522150	Remapped	Perfect	NC_000002.11:g.652 16389_65216390ins9 5	GRCh37.p13	First Pass	NC_000002.11	Chr2	65,216,389	65,216,389

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.

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