A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094528



Internal ID20661568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:118951906..118954490hg38UCSC Ensembl
chr3:118670753..118673337hg19UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg382585
hg192585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356205
Supporting Variants
Samples
Known GenesIGSF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094528
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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