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dbVar

Database of genomic structural variation

nsv7045327

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:2,835,206

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: 6164 SVs from 107 studies. See in: genome view

Submitted genomic34,817,999-37,653,204

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7045327	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	34,817,999	37,653,204
nsv7045327	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	34,857,611	37,692,807

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18780640	inversion	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
nssv18780640	Submitted genomic		NC_000007.14:g.348 17999_37653204inv	GRCh38 (hg38)		NC_000007.14	Chr7	34,817,999	37,653,204
nssv18780640	Remapped	Perfect	NC_000007.13:g.348 57611_37692807inv	GRCh37.p13	First Pass	NC_000007.13	Chr7	34,857,611	37,692,807

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)
nssv18780640	0.059	15557	262870

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