A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2760087



Internal ID17824405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5610262..5669114hg38UCSC Ensembl
Innerchr10:5652225..5711077hg19UCSC Ensembl
Innerchr10:5692231..5751083hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3858853
hg1958853
hg1858853
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975791
Supporting Variants
SamplesHGDP00927
Known GenesASB13
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2760087
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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