A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551518



Internal ID15992241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73873821..73874406hg38UCSC Ensembl
Innerchr10:75633579..75634164hg19UCSC Ensembl
Innerchr10:75303585..75304170hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38586
hg19586
hg18586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv750276
Samples
Known GenesCAMK2G
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551518
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