A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044617



Internal ID19133836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69367906..69392308hg38UCSC Ensembl
Innerchr15:69660245..69684647hg19UCSC Ensembl
Innerchr15:67447299..67471701hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3824403
hg1924403
hg1824403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553663
Samples
Known GenesPAQR5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044617
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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