A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040860



Internal ID19130079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22097038..22206987hg38UCSC Ensembl
Innerchr15:22384989..22494938hg19UCSC Ensembl
Innerchr15:19886353..19996302hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38109950
hg19109950
hg18109950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2395n100
Supporting Variantsnssv3542618
Samples
Known GenesOR4N3P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040860
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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