A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3614948



Internal ID18913229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176177207..176231852hg38UCSC Ensembl
Innerchr3:175894995..175949640hg19UCSC Ensembl
Innerchr3:177377689..177432334hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3854646
hg1954646
hg1854646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009642
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)nssv3614948
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