A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17048354



Internal ID100107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73981972..73989662hg38UCSC Ensembl
chr11:73693017..73700707hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg387691
hg197691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511514
Supporting Variants
Samples
Known GenesUCP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17048354
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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