A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015041



Internal ID18757576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:359178..529515hg38UCSC Ensembl
Innerchr3:400861..571198hg19UCSC Ensembl
Innerchr3:375861..546198hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38170338
hg19170338
hg18170338
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590276
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)nsv1015041
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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