A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051573



Internal ID19140792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73239263..73268468hg38UCSC Ensembl
Innerchr14:73705971..73735176hg19UCSC Ensembl
Innerchr14:72775724..72804929hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3829206
hg1929206
hg1829206
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1932n100
Supporting Variantsnssv3531139
Samples
Known GenesPAPLN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051573
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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