A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993485



Internal ID20560525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67350574..67354288hg38UCSC Ensembl
chr11:67118045..67121759hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg383715
hg193715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469652
Supporting Variants
Samples
Known GenesLOC100130987, POLD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993485
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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