A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569677



Internal ID16357086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62414259..62415506hg38UCSC Ensembl
Innerchr15:62706458..62707705hg19UCSC Ensembl
Innerchr15:60493750..60494997hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381248
hg191248
hg181248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4568n54
Supporting Variantsnssv843907, nssv843904, nssv843901, nssv843898, nssv843903, nssv843900, nssv843905, nssv843908, nssv843902, nssv843899, nssv843906
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569677
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer