A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047793



Internal ID19137012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22108290..22215910hg38UCSC Ensembl
Innerchr15:22396241..22503861hg19UCSC Ensembl
Innerchr15:19897605..20005225hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38107621
hg19107621
hg18107621
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2395n100
Supporting Variantsnssv3542714
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)nsv1047793
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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