A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058158



Internal ID19147377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73123894..73702634hg38UCSC Ensembl
Innerchr18:70791129..71369869hg19UCSC Ensembl
Innerchr18:68942109..69520849hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38578741
hg19578741
hg18578741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3562977
Samples
Known GenesLOC100505817, LOC400655
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058158
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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