A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524176



Internal ID15451469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:81740834..81866890hg38UCSC Ensembl
Innerchr15:82033175..82159231hg19UCSC Ensembl
Innerchr15:79820230..79946286hg18UCSC Ensembl
Innerchr15:79820230..79946286hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38126057
hg19126057
hg18126057
hg17126057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700057
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524176
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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