A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993603



Internal ID20560643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74463013..74463364hg38UCSC Ensembl
chr11:74174058..74174409hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460305
Supporting Variants
Samples
Known GenesKCNE3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993603
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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