A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv749105



Internal ID16043061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64616201..64662787hg38UCSC Ensembl
Innerchr10:66375958..66422544hg19UCSC Ensembl
Innerchr10:66045964..66092550hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3846587
hg1946587
hg1846587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551204
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)nssv749105
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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