A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524996



Internal ID15452289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83107883..83211843hg38UCSC Ensembl
Innerchr8:84020118..84124078hg19UCSC Ensembl
Innerchr8:84182673..84286633hg18UCSC Ensembl
Innerchr8:84182673..84286633hg17UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38103961
hg19103961
hg18103961
hg17103961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701027
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524996
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