A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994128



Internal ID20561168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65678712..65681327hg38UCSC Ensembl
chr11:65446183..65448798hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382616
hg192616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463287
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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