A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552702



Internal ID15993425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133452885..133617534hg38UCSC Ensembl
Innerchr10:135266389..135431038hg19UCSC Ensembl
Innerchr10:135116379..135281028hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38164650
hg19164650
hg18164650
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1486n54
Supporting Variantsnssv762971, nssv762972, nssv1175063
Samples1780854117_A
Known GenesCYP2E1, SCART1, SPRNP1, SYCE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552702
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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