A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042675



Internal ID18785206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:57992383..58115774hg38UCSC Ensembl
Innerchr14:58459101..58582492hg19UCSC Ensembl
Innerchr14:57528854..57652245hg18UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38123392
hg19123392
hg18123392
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531043
Samples
Known GenesC14orf37
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042675
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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