A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551178



Internal ID16338587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:60805285..60828410hg38UCSC Ensembl
Innerchr10:62565043..62588168hg19UCSC Ensembl
Innerchr10:62235049..62258174hg18UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3823126
hg1923126
hg1823126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv748923
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551178
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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