A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552550



Internal ID16339959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133111200..133111885hg38UCSC Ensembl
Innerchr10:134924704..134925389hg19UCSC Ensembl
Innerchr10:134774694..134775379hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38686
hg19686
hg18686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1467n54
Supporting Variantsnssv762026, nssv762009, nssv762010, nssv762011, nssv762019, nssv762012, nssv762021, nssv762008, nssv762032, nssv762029, nssv762030, nssv762025, nssv762023, nssv762013, nssv762016, nssv762033, nssv762031, nssv762024, nssv762017, nssv762028, nssv762022, nssv762015, nssv762014, nssv762027, nssv762020, nssv762018
Samples
Known GenesGPR123
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552550
Frequency
Sample Size17421
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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