A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039101



Internal ID21948444
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 StatusM
Merged Variants
Supporting Variantsnssv17591944
Samples
Known GenesUCP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039101
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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