A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992749



Internal ID20559789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70055963..70057091hg38UCSC Ensembl
chr11:69902069..69903197hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg381129
hg191129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473050
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992749
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00223


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