A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975791



Internal ID18610998
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2760087
SamplesHGDP00927
Known GenesASB13
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975791
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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