A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046125



Internal ID18788656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102526629..102742816hg38UCSC Ensembl
Innerchr14:102992966..103209153hg19UCSC Ensembl
Innerchr14:102062719..102278906hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38216188
hg19216188
hg18216188
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3533559
Samples
Known GenesMIR4309, RCOR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046125
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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