A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039539



Internal ID21948882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28228484..28228568hg38UCSC Ensembl
chr15:28473630..28473714hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604282
Samples
Known GenesHERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039539
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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