A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013515



Internal ID19102733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155347320..155377666hg38UCSC Ensembl
Innerchr3:155065109..155095455hg19UCSC Ensembl
Innerchr3:156547803..156578149hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3830347
hg1930347
hg1830347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606353
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)nsv1013515
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