A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5546995



Internal ID320887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63820879..63820879hg38UCSC Ensembl
chr15:64113078..64113078hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702881
Samples
Known GenesHERC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5546995
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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