A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526484



Internal ID15453777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94650286..94964192hg38UCSC Ensembl
Innerchr6:95360004..95673909hg19UCSC Ensembl
Innerchr6:95416725..95730630hg18UCSC Ensembl
Innerchr6:95416725..95730630hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38313907
hg19313906
hg18313906
hg17313906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702793
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526484
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