A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971901



Internal ID18260432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12897050..12903518hg38UCSC Ensembl
Innerchr10:12939050..12945518hg19UCSC Ensembl
Innerchr10:12979056..12985524hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg386469
hg196469
hg186469
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2759170
SamplesHGDP00998
Known GenesCCDC3
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971901
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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