A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060086



Internal ID19149305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71535310..71646991hg38UCSC Ensembl
Innerchr18:69202546..69314227hg19UCSC Ensembl
Innerchr18:67353526..67465207hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38111682
hg19111682
hg18111682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3723221
Samples
Known GenesLOC100505776
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060086
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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