A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987827



Internal ID20554867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124490868..124491504hg38UCSC Ensembl
chr11:124360764..124361400hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38637
hg19637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457636
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987827
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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