A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053974



Internal ID19143193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28459709..28550848hg38UCSC Ensembl
Innerchr14:28928915..29020054hg19UCSC Ensembl
Innerchr14:27998666..28089805hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3891140
hg1991140
hg1891140
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528582
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053974
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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