A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3604226



Internal ID18902507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99225602..99279362hg38UCSC Ensembl
Innerchr3:98944446..98998206hg19UCSC Ensembl
Innerchr3:100427136..100480896hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3853761
hg1953761
hg1853761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013972
Supporting Variants
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)nssv3604226
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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