A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094687



Internal ID20661727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159295163..159307148hg38UCSC Ensembl
chr3:159012952..159024937hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg3811986
hg1911986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366467
Supporting Variants
Samples
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094687
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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