A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975059



Internal ID18263581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8015970..8025658hg38UCSC Ensembl
Innerchr10:8057933..8067621hg19UCSC Ensembl
Innerchr10:8097939..8107627hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg389689
hg199689
hg189689
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2765082
SamplesHGDP00998
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975059
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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