A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498207



Internal ID20871415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61919875..62253423hg38UCSC Ensembl
chr15:62212074..62545622hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38333549
hg19333549
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195128
Samples
Known GenesC2CD4A, C2CD4B, VPS13C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498207
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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