A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552263



Internal ID16339672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122585191..122598111hg38UCSC Ensembl
Innerchr10:124344707..124357627hg19UCSC Ensembl
Innerchr10:124334697..124347617hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3812921
hg1912921
hg1812921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1410n54
Supporting Variantsnssv760450
Samples
Known GenesDMBT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552263
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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