A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570160



Internal ID16357569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77716746..77719066hg38UCSC Ensembl
Innerchr15:78009088..78011408hg19UCSC Ensembl
Innerchr15:75796143..75798463hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg382321
hg192321
hg182321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4663n54
Supporting Variantsnssv847352
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570160
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