A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv755892



Internal ID16049848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94402684..94403555hg38UCSC Ensembl
Innerchr10:96162441..96163312hg19UCSC Ensembl
Innerchr10:96152431..96153302hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38872
hg19872
hg18872
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551952
Supporting Variants
Samples
Known GenesTBC1D12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv755892
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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