A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047246



Internal ID18789777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58083408..58414959hg38UCSC Ensembl
Innerchr15:58375607..58707158hg19UCSC Ensembl
Innerchr15:56162899..56494450hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38331552
hg19331552
hg18331552
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3717943
Samples
Known GenesAQP9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047246
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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