A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048707



Internal ID18791238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:788499..869594hg38UCSC Ensembl
Innerchr10:834439..915534hg19UCSC Ensembl
Innerchr10:824439..905534hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3881096
hg1981096
hg1881096
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3501317
Samples
Known GenesLARP4B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048707
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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