A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551099



Internal ID16338508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56798193..56858319hg38UCSC Ensembl
Innerchr10:58557953..58618079hg19UCSC Ensembl
Innerchr10:58227959..58288085hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3860127
hg1960127
hg1860127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv748607
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551099
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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