A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv762040



Internal ID16055996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133111200..133111936hg38UCSC Ensembl
Innerchr10:134924704..134925440hg19UCSC Ensembl
Innerchr10:134774694..134775430hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38737
hg19737
hg18737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552551
Supporting Variants
Samples
Known GenesGPR123
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv762040
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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