A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519810



Internal ID15447103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:139421651..139422670hg38UCSC Ensembl
Innerchr6:139742788..139743807hg19UCSC Ensembl
Innerchr6:139784481..139785500hg18UCSC Ensembl
Innerchr6:139784481..139785500hg17UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg381020
hg191020
hg181020
hg171020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697063
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519810
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