A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047686



Internal ID19136905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5106261..5143390hg38UCSC Ensembl
Innerchr10:5148453..5185582hg19UCSC Ensembl
Innerchr10:5138453..5175582hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3837130
hg1937130
hg1837130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707674
Samples
Known GenesAKR1C3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047686
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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