A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998340



Internal ID19157876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164330163..164607592hg38UCSC Ensembl
Innerchr3:164047951..164325380hg19UCSC Ensembl
Innerchr3:165530645..165808074hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38277430
hg19277430
hg18277430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3738251
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)nsv998340
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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