A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210384



Internal ID20777424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159366202..159459657hg38UCSC Ensembl
chr3:159083991..159177446hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg3893456
hg1993456
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359365
Supporting Variants
Samples
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210384
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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