A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608037



Internal ID21800084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:82671799..82671799hg38UCSC Ensembl
chr12:83065578..83065578hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091478
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608037
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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