A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3723217



Internal ID19021498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:70465717..70499331hg38UCSC Ensembl
Innerchr18:68132953..68166567hg19UCSC Ensembl
Innerchr18:66283933..66317547hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3833615
hg1933615
hg1833615
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061526
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3723217
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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