A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409405



Internal ID21066958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34426869..34963561hg38UCSC Ensembl
chr6:34394646..34931338hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38536693
hg19536693
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226876
Samples
Known GenesANKS1A, C6orf106, PACSIN1, SNRPC, SPDEF, TAF11, UHRF1BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409405
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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