A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570397



Internal ID16011120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90740512..90747520hg38UCSC Ensembl
Innerchr15:91283743..91290750hg19UCSC Ensembl
Innerchr15:89084747..89091754hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg387009
hg197008
hg187008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv848210
Samples
Known GenesBLM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570397
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