A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012315



Internal ID18754848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..105837hg38UCSC Ensembl
Innerchr3:60333..147520hg19UCSC Ensembl
Innerchr3:35333..122520hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3887183
hg1987188
hg1887188
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4605n100
Supporting Variantsnssv3590192, nssv3590191, nssv3590193
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)nsv1012315
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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