A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999953



Internal ID19159489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75458231..75832110hg38UCSC Ensembl
Innerchr3:75507382..75881261hg19UCSC Ensembl
Innerchr3:75590072..75963951hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38373880
hg19373880
hg18373880
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4773n100
Supporting Variantsnssv3733729
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)nsv999953
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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