A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002746



Internal ID18745278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3874041..4047628hg38UCSC Ensembl
Innerchr3:3915725..4089312hg19UCSC Ensembl
Innerchr3:3890725..4064312hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38173588
hg19173588
hg18173588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4638n100
Supporting Variantsnssv3739550
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)nsv1002746
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