A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528132



Internal ID15455425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8085234..8087097hg38UCSC Ensembl
Innerchr1:8145294..8147157hg19UCSC Ensembl
Innerchr1:8067881..8069744hg18UCSC Ensembl
Innerchr1:8079560..8081423hg17UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg381864
hg191864
hg181864
hg171864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704677
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528132
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