A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413769



Internal ID21071322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41943080..41960366hg38UCSC Ensembl
chr6:41910818..41928104hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3817287
hg1917287
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230970
Samples
Known GenesCCND3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413769
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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