A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv750259



Internal ID16044215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70961606..70983197hg38UCSC Ensembl
Innerchr10:72721363..72742954hg19UCSC Ensembl
Innerchr10:72391369..72412960hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3821592
hg1921592
hg1821592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551497
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)nssv750259
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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