A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994792



Internal ID20561832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85625356..85625750hg38UCSC Ensembl
chr11:85336400..85336794hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456445
Supporting Variants
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994792
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00076


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