A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006735



Internal ID18749266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:214575..294771hg38UCSC Ensembl
Innerchr3:256258..336454hg19UCSC Ensembl
Innerchr3:231258..311454hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3880197
hg1980197
hg1880197
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4614n100
Supporting Variantsnssv3590268
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)nsv1006735
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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