A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975800



Internal ID18611007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87768067..87771651hg38UCSC Ensembl
Innerchr10:89527824..89531408hg19UCSC Ensembl
Innerchr10:89517804..89521388hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg383585
hg193585
hg183585
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2757424
SamplesHGDP00998
Known GenesATAD1
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975800
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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