A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2760172



Internal ID17833878
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 Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv976263
Supporting Variants
SamplesHGDP00998
Known GenesTPP2
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2760172
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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