A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058545



Internal ID19147764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:64825732..64892169hg38UCSC Ensembl
Innerchr18:62492968..62559405hg19UCSC Ensembl
Innerchr18:60643948..60710385hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3866438
hg1966438
hg1866438
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565638
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)nsv1058545
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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