A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982895



Internal ID18271404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24604970..24610024hg38UCSC Ensembl
Innerchr10:24893899..24898953hg19UCSC Ensembl
Innerchr10:24933905..24938959hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg385055
hg195055
hg185055
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758935
SamplesHGDP00665
Known GenesARHGAP21
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982895
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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