A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036319



Internal ID19125538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76140482..76197614hg38UCSC Ensembl
Innerchr15:76432823..76489955hg19UCSC Ensembl
Innerchr15:74219878..74277010hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3857133
hg1957133
hg1857133
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2623n100
Supporting Variantsnssv3553709
Samples
Known GenesC15orf27
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036319
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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