A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723170



Internal ID146836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37262874..37268874hg38UCSC Ensembl
chr19:37753776..37759776hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145399
Supporting Variants
Samples
Known GenesLOC284412
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723170
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000821


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