A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550223



Internal ID16337632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24432633..24483795hg38UCSC Ensembl
Innerchr10:24721562..24772724hg19UCSC Ensembl
Innerchr10:24761568..24812730hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3851163
hg1951163
hg1851163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173862
Samples1780862484_A
Known GenesKIAA1217
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550223
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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