A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552517



Internal ID16339926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132378307..132436969hg38UCSC Ensembl
Innerchr10:134191811..134250473hg19UCSC Ensembl
Innerchr10:134041801..134100463hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3858663
hg1958663
hg1858663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174733
SamplesHGDP01036
Known GenesLRRC27, PWWP2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552517
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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