A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551839



Internal ID15992562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:88575078..88662379hg38UCSC Ensembl
Innerchr10:90334835..90422136hg19UCSC Ensembl
Innerchr10:90324815..90412116hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3887302
hg1987302
hg1887302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv753222
Samples
Known GenesLIPJ, RNLS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551839
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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