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dbVar

Database of genomic structural variation

nsv6517656

Organism: Homo sapiens

Study:nstd223 (Sedlazeck et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:611

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: 170 SVs from 21 studies. See in: genome view

Submitted genomic79,022,064-79,022,674

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6517656	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	79,022,064	79,022,674
nsv6517656	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	77,018,146	77,018,756

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18038151	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18038151	Submitted genomic		NC_000017.11:g.790 22064_79022674del	GRCh38 (hg38)		NC_000017.11	Chr17	79,022,064	79,022,674
nssv18038151	Remapped	Perfect	NC_000017.10:g.770 18146_77018756del	GRCh37.p13	First Pass	NC_000017.10	Chr17	77,018,146	77,018,756

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)
nssv18038151	<0.001	3	39058

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