A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv760299



Internal ID16054255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121672674..121701552hg38UCSC Ensembl
Innerchr10:123432188..123461066hg19UCSC Ensembl
Innerchr10:123422178..123451056hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3828879
hg1928879
hg1828879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552234
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)nssv760299
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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