A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039515



Internal ID21948858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102135224..102135387hg38UCSC Ensembl
chr14:102601561..102601724hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600332
Samples
Known GenesHSP90AA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039515
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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