A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520297



Internal ID15447590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:137430091..137430229hg38UCSC Ensembl
Innerchr6:137751228..137751366hg19UCSC Ensembl
Innerchr6:137792921..137793059hg18UCSC Ensembl
Innerchr6:137792921..137793059hg17UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38139
hg19139
hg18139
hg17139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688246, nssv662515
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520297
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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