A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570235



Internal ID16357644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:80541802..80598985hg38UCSC Ensembl
Innerchr15:80834143..80891326hg19UCSC Ensembl
Innerchr15:78621198..78678381hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3857184
hg1957184
hg1857184
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv847551
Samples
Known GenesARNT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570235
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