A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993896



Internal ID20560936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74025447..74026724hg38UCSC Ensembl
chr11:73736492..73737769hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg381278
hg191278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475332
Supporting Variants
Samples
Known GenesC2CD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993896
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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