A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976263



Internal ID18611470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:102649871..102655303hg38UCSC Ensembl
Innerchr13:103302221..103307653hg19UCSC Ensembl
Innerchr13:102100222..102105654hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg385433
hg195433
hg185433
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2760172
SamplesHGDP00998
Known GenesTPP2
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976263
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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