A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042514



Internal ID19131733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76545880..76614041hg38UCSC Ensembl
Innerchr15:76838221..76906382hg19UCSC Ensembl
Innerchr15:74625276..74693437hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3868162
hg1968162
hg1868162
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3717962
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)nsv1042514
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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