A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552292



Internal ID16339701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125362698..125410838hg38UCSC Ensembl
Innerchr10:127051267..127099407hg19UCSC Ensembl
Innerchr10:127041257..127089397hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3848141
hg1948141
hg1848141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv760494
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552292
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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