A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044438



Internal ID18786969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41267962..41453282hg38UCSC Ensembl
Innerchr15:41560160..41745480hg19UCSC Ensembl
Innerchr15:39347452..39532772hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38185321
hg19185321
hg18185321
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2580n100
Supporting Variantsnssv3552255
Samples
Known GenesCHP1, NDUFAF1, NUSAP1, OIP5, OIP5-AS1, RTF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044438
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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