A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15202531



Internal ID21341341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73563830..73563830hg38UCSC Ensembl
chr6:74273553..74273553hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3952643
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15202531
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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