A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052767



Internal ID19141986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74110994..74139888hg38UCSC Ensembl
Innerchr14:74577697..74606591hg19UCSC Ensembl
Innerchr14:73647450..73676344hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3828895
hg1928895
hg1828895
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1940n100
Supporting Variantsnssv3531202
Samples
Known GenesLIN52
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052767
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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