A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995249



Internal ID20562289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93769056..93774896hg38UCSC Ensembl
chr11:93502222..93508062hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385841
hg195841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472338
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995249
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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