A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550126



Internal ID16337535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:18981139..19283800hg38UCSC Ensembl
Innerchr10:19270068..19572729hg19UCSC Ensembl
Innerchr10:19310074..19612735hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38302662
hg19302662
hg18302662
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744282
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550126
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