A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691424



Internal ID15428076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:122876930..122898598hg38UCSC Ensembl
Innerchr3:122595777..122617445hg19UCSC Ensembl
Innerchr3:124078467..124100135hg18UCSC Ensembl
Innerchr3:124078467..124100135hg17UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg3821669
hg1921669
hg1821669
hg1721669
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517377
Supporting Variants
Samples
Known GenesDIRC2, LOC100129550
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691424
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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