A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404490



Internal ID21062043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34815416..34997961hg38UCSC Ensembl
chr6:34783193..34965738hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38182546
hg19182546
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229611
Samples
Known GenesANKS1A, TAF11, UHRF1BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404490
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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