A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552255



Internal ID15992978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122522412..122617922hg38UCSC Ensembl
Innerchr10:124281928..124377438hg19UCSC Ensembl
Innerchr10:124271918..124367428hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3895511
hg1995511
hg1895511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv760429
Samples
Known GenesDMBT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552255
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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