A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv762200



Internal ID16056156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133199790..133247360hg38UCSC Ensembl
Innerchr10:135013294..135060864hg19UCSC Ensembl
Innerchr10:134863284..134910855hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3847571
hg1947571
hg1847572
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552584
Supporting Variants
Samples
Known GenesKNDC1, MIR202HG, UTF1, VENTX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv762200
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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