A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5496953



Internal ID274016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71584155..71584895hg38UCSC Ensembl
chr11:71295201..71295941hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5496953
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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