A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992599



Internal ID20559639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6693620..6695970hg38UCSC Ensembl
chr11:6714851..6717201hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382351
hg192351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444163
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992599
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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