A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568742



Internal ID16356151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30294824..30371327hg38UCSC Ensembl
Innerchr15:30587027..30663530hg19UCSC Ensembl
Innerchr15:28374319..28450822hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3876504
hg1976504
hg1876504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4421n54
Supporting Variantsnssv839470
Samples
Known GenesCHRFAM7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568742
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