A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044603



Internal ID19133822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76153348..76192640hg38UCSC Ensembl
Innerchr15:76445689..76484981hg19UCSC Ensembl
Innerchr15:74232744..74272036hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3839293
hg1939293
hg1839293
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2624n100
Supporting Variantsnssv3553725, nssv3553726
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)nsv1044603
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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