A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552587



Internal ID16339996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133255089..133303529hg38UCSC Ensembl
Innerchr10:135068593..135117033hg19UCSC Ensembl
Innerchr10:134918584..134967023hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3848441
hg1948441
hg1848440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174738
SamplesHGDP00602
Known GenesADAM8, TUBGCP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552587
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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