A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17564060



Internal ID21888415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39096566..39096714hg38UCSC Ensembl
chr6:39064342..39064490hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009850
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17564060
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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