A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091478



Internal ID22000711
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 StatusM
Merged Variants
Supporting Variantsnssv17608037
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091478
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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