A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993961



Internal ID20561001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82122992..82344581hg38UCSC Ensembl
chr11:81834034..82055623hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38221590
hg19221590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472949
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993961
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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