A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003234



Internal ID18745765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4298679..4344910hg38UCSC Ensembl
Innerchr3:4340363..4386594hg19UCSC Ensembl
Innerchr3:4315363..4361594hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3846232
hg1946232
hg1846232
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3591634
Samples
Known GenesSETMAR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003234
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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