A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3733738



Internal ID19032019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75465245..75757215hg38UCSC Ensembl
Innerchr3:75514396..75806366hg19UCSC Ensembl
Innerchr3:75597086..75889056hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38291971
hg19291971
hg18291971
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013154
Supporting Variants
Samples
Known GenesFLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, ZNF717
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3733738
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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