A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552585



Internal ID16339994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133209368..133247368hg38UCSC Ensembl
Innerchr10:135022872..135060872hg19UCSC Ensembl
Innerchr10:134872862..134910863hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3838001
hg1938001
hg1838002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1474n54
Supporting Variantsnssv762201
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)nsv552585
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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