A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994042



Internal ID20561082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83126501..83132000hg38UCSC Ensembl
chr11:82837543..82843042hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473931
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994042
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00072


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