A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007886



Internal ID18750417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21944199..21976549hg38UCSC Ensembl
Innerchr3:21985691..22018041hg19UCSC Ensembl
Innerchr3:21960695..21993045hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3832351
hg1932351
hg1832351
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4696n100
Supporting Variantsnssv3589474, nssv3589473, nssv3589472
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)nsv1007886
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