A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066205



Internal ID19155424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:67588657..68009670hg38UCSC Ensembl
Innerchr18:65255894..65676907hg19UCSC Ensembl
Innerchr18:63406874..63827887hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38421014
hg19421014
hg18421014
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3386n100
Supporting Variantsnssv3566442
Samples
Known GenesLOC643542
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066205
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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