A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023811



Internal ID21933154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63788770..63789644hg38UCSC Ensembl
chr15:64080969..64081843hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38875
hg19875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605200
Samples
Known GenesHERC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023811
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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