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dbVar

Database of genomic structural variation

nsv5515582

Organism: Homo sapiens

Study:nstd206 (Byrska-Bishop et al. 2022)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:55

Publication(s):Byrska-Bishop et al. 2022

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: 92 SVs from 18 studies. See in: genome view

Submitted genomic10,436,469-10,436,523

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5515582	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	10,436,469	10,436,523
nsv5515582	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	10,547,145	10,547,199

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17721319	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17721319	Submitted genomic		NC_000019.10:g.104 36469_10436523del	GRCh38 (hg38)		NC_000019.10	Chr19	10,436,469	10,436,523
nssv17721319	Remapped	Perfect	NC_000019.9:g.1054 7145_10547199del	GRCh37.p13	First Pass	NC_000019.9	Chr19	10,547,145	10,547,199

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)
nssv17721319	<0.001	1	6404

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