A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008604



Internal ID18751135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..327088hg38UCSC Ensembl
Innerchr3:60333..368771hg19UCSC Ensembl
Innerchr3:35333..343771hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38308434
hg19308439
hg18308439
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4608n100
Supporting Variantsnssv3590211
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)nsv1008604
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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