A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591944



Internal ID21783987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73981974..73984476hg38UCSC Ensembl
chr11:73693019..73695521hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382503
hg192503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039101
Supporting Variants
Samples
Known GenesUCP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591944
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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