A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982893



Internal ID18618088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12183171..12186548hg38UCSC Ensembl
Innerchr10:12225170..12228547hg19UCSC Ensembl
Innerchr10:12265176..12268553hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383378
hg193378
hg183378
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2762102
SamplesHGDP00998
Known GenesNUDT5
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982893
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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