A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv760797



Internal ID16054753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:129943340..130004269hg38UCSC Ensembl
Innerchr10:131741604..131802533hg19UCSC Ensembl
Innerchr10:131631594..131692523hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3860930
hg1960930
hg1860930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552315
Supporting Variants
Samples
Known GenesEBF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv760797
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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