A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999173



Internal ID19158709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99225602..99288842hg38UCSC Ensembl
Innerchr3:98944446..99007686hg19UCSC Ensembl
Innerchr3:100427136..100490376hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3863241
hg1963241
hg1863241
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4828n100
Supporting Variantsnssv3604227, nssv3604228
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)nsv999173
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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