A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552577



Internal ID16339986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133174792..133184562hg38UCSC Ensembl
Innerchr10:134988296..134998066hg19UCSC Ensembl
Innerchr10:134838286..134848056hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg389771
hg199771
hg189771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv762193
Samples
Known GenesKNDC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552577
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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