A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv751729



Internal ID16045685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76585909..76608495hg38UCSC Ensembl
Innerchr10:78345667..78368253hg19UCSC Ensembl
Innerchr10:78015673..78038259hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3822587
hg1922587
hg1822587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551547
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)nssv751729
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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