A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552644



Internal ID16340053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133328068..133402966hg38UCSC Ensembl
Innerchr10:135141572..135216470hg19UCSC Ensembl
Innerchr10:134991562..135066460hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3874899
hg1974899
hg1874899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175015
Samples1780854339_A
Known GenesCALY, ECHS1, FUOM, MIR3944, MTG1, PAOX, PRAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552644
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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