A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001867



Internal ID18744398
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 StatusM
Merged Variants
Supporting Variantsnssv3590266
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)nsv1001867
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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