A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037282



Internal ID19126501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76566968..76603422hg38UCSC Ensembl
Innerchr15:76859309..76895763hg19UCSC Ensembl
Innerchr15:74646364..74682818hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3836455
hg1936455
hg1836455
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2627n100
Supporting Variantsnssv3553746, nssv3553747
Samples
Known GenesSCAPER
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037282
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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