A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045155



Internal ID18787686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4830047..5169355hg38UCSC Ensembl
Innerchr10:4872239..5211318hg19UCSC Ensembl
Innerchr10:4862239..5201318hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38339309
hg19339080
hg18339080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707671, nssv3494130
Samples
Known GenesAKR1C1, AKR1C2, AKR1C3, AKR1C6P, AKR1CL1, AKR1E2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045155
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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