A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577762



Internal ID21769805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31177975..31178369hg38UCSC Ensembl
chr11:31199522..31199916hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035982
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577762
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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