A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628083



Internal ID21820130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:135414..135633hg38UCSC Ensembl
chr11:190949..191168hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038240
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628083
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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