A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986604



Internal ID20553644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11002024..11002157hg38UCSC Ensembl
chr11:11023571..11023704hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449640
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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