A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009759



Internal ID18752290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46760459..46804334hg38UCSC Ensembl
Innerchr3:46801949..46845824hg19UCSC Ensembl
Innerchr3:46776953..46820828hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3843876
hg1943876
hg1843876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4736n100
Supporting Variantsnssv3593779
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009759
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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