A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995546



Internal ID20562586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95145630..95148259hg38UCSC Ensembl
chr11:94878794..94881423hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg382630
hg192630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462916
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995546
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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