A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047903



Internal ID99799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63068994..63076819hg38UCSC Ensembl
chr11:62836466..62844291hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg387826
hg197826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504721
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047903
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.010775


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