A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043877



Internal ID19133096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74103225..74131604hg38UCSC Ensembl
Innerchr14:74569928..74598307hg19UCSC Ensembl
Innerchr14:73639681..73668060hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3828380
hg1928380
hg1828380
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1939n100
Supporting Variantsnssv3531171
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)nsv1043877
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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