A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047775



Internal ID18790306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52529853..52620031hg38UCSC Ensembl
Innerchr15:52822050..52912228hg19UCSC Ensembl
Innerchr15:50609342..50699520hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3890179
hg1990179
hg1890179
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552405
Samples
Known GenesARPP19, FAM214A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047775
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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