A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051915



Internal ID19141134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:59055575..59078477hg38UCSC Ensembl
Innerchr14:59522293..59545195hg19UCSC Ensembl
Innerchr14:58592046..58614948hg18UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3822903
hg1922903
hg1822903
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531044
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)nsv1051915
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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