A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039386



Internal ID18781917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4966191..5344882hg38UCSC Ensembl
Innerchr10:5008383..5386845hg19UCSC Ensembl
Innerchr10:4998383..5376845hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38378692
hg19378463
hg18378463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3486246
Samples
Known GenesAKR1C1, AKR1C2, AKR1C3, AKR1C4, AKR1CL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039386
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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