A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590266



Internal ID18541861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:193194..252963hg38UCSC Ensembl
Innerchr3:234877..294646hg19UCSC Ensembl
Innerchr3:209877..269646hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3859770
hg1959770
hg1859770
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001867
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)nssv3590266
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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