A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590269



Internal ID18541864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:219969..284854hg38UCSC Ensembl
Innerchr3:261652..326537hg19UCSC Ensembl
Innerchr3:236652..301537hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3864886
hg1964886
hg1864886
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002942
Supporting Variants
Samples
Known GenesCHL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3590269
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