A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3935637



Internal ID21355707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122747738..122747738hg38UCSC Ensembl
chr3:122466585..122466585hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189848
SamplesHG002
Known GenesHSPBAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3935637
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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