A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989380



Internal ID20556420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15283247..15283774hg38UCSC Ensembl
chr11:15304793..15305320hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452404
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989380
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00045


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