A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976762



Internal ID18611968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:10800032..10802707hg38UCSC Ensembl
Innerchr12:10952631..10955306hg19UCSC Ensembl
Innerchr12:10843898..10846573hg18UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg382676
hg192676
hg182676
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2761650
SamplesHGDP00665
Known GenesTAS2R7
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976762
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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