A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989882



Internal ID20556922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35691913..35696355hg38UCSC Ensembl
chr11:35713461..35717903hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg384443
hg194443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459764
Supporting Variants
Samples
Known GenesTRIM44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989882
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00176


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