A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015134



Internal ID18757669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:129984722..130080812hg38UCSC Ensembl
Innerchr3:129703565..129799655hg19UCSC Ensembl
Innerchr3:131186255..131282345hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3896091
hg1996091
hg1896091
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4860n100
Supporting Variantsnssv3603541, nssv3603542
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)nsv1015134
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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