A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3594611



Internal ID18546206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:64465605..64532445hg38UCSC Ensembl
Innerchr3:64451281..64518121hg19UCSC Ensembl
Innerchr3:64426321..64493161hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3866841
hg1966841
hg1866841
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014598
Supporting Variants
Samples
Known GenesADAMTS9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3594611
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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