A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521689



Internal ID15448982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:32401116..32409679hg38UCSC Ensembl
Innerchr1:32866717..32875280hg19UCSC Ensembl
Innerchr1:32639304..32647867hg18UCSC Ensembl
Innerchr1:32535810..32544373hg17UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg388564
hg198564
hg188564
hg178564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698309
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521689
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