A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994287



Internal ID20561327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75931498..75936333hg38UCSC Ensembl
chr11:75642542..75647377hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg384836
hg194836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458559
Supporting Variants
Samples
Known GenesUVRAG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994287
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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