A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995460



Internal ID20562500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96377201..96378600hg38UCSC Ensembl
chr11:96110365..96111764hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471321
Supporting Variants
Samples
Known GenesCCDC82
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995460
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0006


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