A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046434



Internal ID98757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71504066..71537625hg38UCSC Ensembl
chr11:71215112..71248671hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3833560
hg1933560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504128
Supporting Variants
Samples
Known GenesKRTAP5-7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046434
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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