A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552024



Internal ID15992747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97366492..97414113hg38UCSC Ensembl
Innerchr10:99126249..99173870hg19UCSC Ensembl
Innerchr10:99116239..99163860hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3847622
hg1947622
hg1847622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1369n54
Supporting Variantsnssv1174568
SamplesHGDP01060
Known GenesRRP12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552024
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