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dbVar

Database of genomic structural variation

nsv5556604

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:334,818

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: 1085 SVs from 70 studies. See in: genome view

Submitted genomic38,269,810-38,604,627

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5556604	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	38,269,810	38,604,627
nsv5556604	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	38,760,450	39,095,267

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17723247	sequence alteration	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17723247	Submitted genomic		GRCh38 (hg38)		NC_000019.10	Chr19	38,269,810	38,604,627
nssv17723247	Remapped	Perfect	GRCh37.p13	First Pass	NC_000019.9	Chr19	38,760,450	39,095,267

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)
nssv17723247	<0.001	4	6404

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