A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv763030



Internal ID16056986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133762002..133776587hg38UCSC Ensembl
Innerchr10:135499327..135513912hg19UCSC Ensembl
Innerchr10:135349317..135363902hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3814586
hg1914586
hg1814586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552755
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv763030
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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