A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697482



Internal ID15087448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:95905623..98010484hg38UCSC Ensembl
Innerchr3:95624467..97729328hg19UCSC Ensembl
Innerchr3:97107157..99212018hg18UCSC Ensembl
Innerchr3:97107157..99212018hg17UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg382104862
hg192104862
hg182104862
hg172104862
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520553
Supporting Variants
Samples
Known GenesARL6, CRYBG3, EPHA6, GABRR3, MINA, MIR8060
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697482
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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