A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987613



Internal ID20554654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122043566..122044113hg38UCSC Ensembl
chr11:121914274..121914821hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38548
hg19548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474557
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987613
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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