A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552574



Internal ID16339983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133140872..133249523hg38UCSC Ensembl
Innerchr10:134954376..135063027hg19UCSC Ensembl
Innerchr10:134804366..134913018hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38108652
hg19108652
hg18108653
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv762183
Samples
Known GenesKNDC1, MIR202, MIR202HG, UTF1, VENTX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552574
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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