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dbVar

Database of genomic structural variation

nsv4563813

Organism: Homo sapiens

Study:nstd166 (gnomAD Structural Variants)
Variant Type:sequence alteration
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:108,837

Description:complex variant
Publication(s):gnomAD_Structural_Variants

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: 192 SVs from 16 studies. See in: genome view

Remapped(Score: Perfect):76,686,154-76,794,990

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4563813	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	76,686,154	76,794,990
nsv4563813	Submitted genomic		GRCh37.p13	Primary Assembly		NC_000017.10	Chr17	74,682,236	74,791,072

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15788576	sequence alteration	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15788576	Remapped	Perfect	GRCh38.p12	First Pass	NC_000017.11	Chr17	76,686,154	76,794,990
nssv15788576	Submitted genomic		GRCh37.p13		NC_000017.10	Chr17	74,682,236	74,791,072

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)
nssv15788576	<0.001	3	21666

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