A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993845



Internal ID20560885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64318001..64319700hg38UCSC Ensembl
chr11:64085473..64087172hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474584
Supporting Variants
Samples
Known GenesPRDX5, TRMT112
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993845
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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