A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042255



Internal ID19131474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26314685..26360065hg38UCSC Ensembl
Innerchr14:26783891..26829271hg19UCSC Ensembl
Innerchr14:25853731..25899111hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3845381
hg1945381
hg1845381
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528538
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)nsv1042255
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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