A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552557



Internal ID16339966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133111251..133111829hg38UCSC Ensembl
Innerchr10:134924755..134925333hg19UCSC Ensembl
Innerchr10:134774745..134775323hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38579
hg19579
hg18579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1467n54
Supporting Variantsnssv762112, nssv762105, nssv762115, nssv762119, nssv762113, nssv762110, nssv762117, nssv762108, nssv762114, nssv762095, nssv762099, nssv762101, nssv762098, nssv762103, nssv762125, nssv762120, nssv762100, nssv762096, nssv762122, nssv762104, nssv762124, nssv762118, nssv762107, nssv762121, nssv762116, nssv762106, nssv762097, nssv762102, nssv762109, nssv762123, nssv762111
Samples
Known GenesGPR123
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552557
Frequency
Sample Size17421
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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