A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591643



Internal ID21783686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67063980..67064280hg38UCSC Ensembl
chr11:66831451..66831751hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036600
Supporting Variants
Samples
Known GenesRHOD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591643
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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