A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004723



Internal ID18747254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155763308..155774388hg38UCSC Ensembl
Innerchr3:155481097..155492177hg19UCSC Ensembl
Innerchr3:156963791..156974871hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3811081
hg1911081
hg1811081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4927n100
Supporting Variantsnssv3606368, nssv3606362, nssv3606367, nssv3741552, nssv3606364, nssv3606369, nssv3606380, nssv3606373, nssv3606374, nssv3606360, nssv3606379, nssv3606363, nssv3606375, nssv3606365, nssv3741551, nssv3741550, nssv3606377, nssv3606371, nssv3606359, nssv3606376, nssv3741553, nssv3606361, nssv3606372, nssv3606358, nssv3606378, nssv3606370, nssv3606366
Samples
Known GenesC3orf33
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004723
Frequency
Sample Size29084
Observed Gain27
Observed Loss0
Observed Complex0
Frequencyn/a


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