A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043739



Internal ID96887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38619600..38619664hg38UCSC Ensembl
chr11:38641150..38641214hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510691
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043739
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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