A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001115



Internal ID18743646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3969405..4188819hg38UCSC Ensembl
Innerchr3:4011089..4230503hg19UCSC Ensembl
Innerchr3:3986089..4205503hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38219415
hg19219415
hg18219415
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4641n100
Supporting Variantsnssv3739553
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)nsv1001115
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