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dbVar

Database of genomic structural variation

nsv5560911

Organism: Homo sapiens

Study:nstd206 (Byrska-Bishop et al. 2022)
Variant Type:sequence alteration
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:457,101

Description:complex variant
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: 3116 SVs from 109 studies. See in: genome view

Submitted genomic16,483,139-16,940,239

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5560911	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	16,483,139	16,940,239
nsv5560911	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	16,809,634	17,266,734

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16896611	sequence alteration	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16896611	Submitted genomic		GRCh38 (hg38)		NC_000001.11	Chr1	16,483,139	16,940,239
nssv16896611	Remapped	Perfect	GRCh37.p13	First Pass	NC_000001.10	Chr1	16,809,634	17,266,734

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)
nssv16896611	<0.001	5	6404

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