A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997846



Internal ID18810696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:96522724..96689179hg38UCSC Ensembl
Innerchr3:96241568..96408023hg19UCSC Ensembl
Innerchr3:97724258..97890713hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38166456
hg19166456
hg18166456
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3603305
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)nsv997846
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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