A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv750266



Internal ID15697536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:71971684..71984712hg38UCSC Ensembl
Innerchr10:73731442..73744470hg19UCSC Ensembl
Innerchr10:73401448..73414476hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3813029
hg1913029
hg1813029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551509
Supporting Variants
Samples
Known GenesCHST3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv750266
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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