A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550234



Internal ID16337643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26711629..26712885hg38UCSC Ensembl
Innerchr10:27000558..27001814hg19UCSC Ensembl
Innerchr10:27040564..27041820hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg381257
hg191257
hg181257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744766, nssv744784, nssv744768, nssv744758, nssv744746, nssv744765, nssv744761, nssv744760, nssv744781, nssv744771, nssv744749, nssv744751, nssv744780, nssv744782, nssv744776, nssv744767, nssv744763, nssv744762, nssv744747, nssv744745, nssv744753, nssv744772, nssv744769, nssv744764, nssv744748, nssv744773, nssv744759, nssv744778, nssv744779, nssv744744, nssv744775, nssv744774, nssv744750, nssv744752, nssv744756, nssv744783, nssv744770, nssv744757, nssv744777, nssv744754, nssv744755
Samples
Known GenesPDSS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550234
Frequency
Sample Size17421
Observed Gain0
Observed Loss41
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer