A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993900



Internal ID20560940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74125482..74125769hg38UCSC Ensembl
chr11:73836527..73836814hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467805
Supporting Variants
Samples
Known GenesC2CD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00012


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