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

dbVar

Database of genomic structural variation

nsv6807019

Organism: Homo sapiens

Study:nstd229 (Jun et al. 2023)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:469,780

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: 1296 SVs from 86 studies. See in: genome view

Submitted genomic10,525,147-10,994,926

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6807019	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	10,525,147	10,994,926
nsv6807019	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	10,564,774	11,034,553

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18717653	duplication	Sequencing	Split read and paired-end mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18717653	Submitted genomic		NC_000007.14:g.105 25147_10994926dup	GRCh38 (hg38)		NC_000007.14	Chr7	10,525,147	10,994,926
nssv18717653	Remapped	Perfect	NC_000007.13:g.105 64774_11034553dup	GRCh37.p13	First Pass	NC_000007.13	Chr7	10,564,774	11,034,553

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv18717653	4e-06	1	275598

You are here: NCBI