A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993445



Internal ID20560486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57741401..57741900hg38UCSC Ensembl
chr11:57508873..57509372hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464947
Supporting Variants
Samples
Known GenesC11orf31, TMX2-CTNND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993445
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.06563


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