A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366564



Internal ID21024117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159735130..159736097hg38UCSC Ensembl
chr3:159452919..159453886hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38968
hg19968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094720
Samples
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366564
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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