A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551561



Internal ID15992284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:78349364..79336832hg38UCSC Ensembl
Innerchr10:80109121..81096589hg19UCSC Ensembl
Innerchr10:79779127..80766595hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38987469
hg19987469
hg18987469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174547
Samples1780862456_A
Known GenesZMIZ1, ZMIZ1-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551561
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