A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056690



Internal ID18799221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76794730..76903712hg38UCSC Ensembl
Innerchr18:74506686..74615668hg19UCSC Ensembl
Innerchr18:72635674..72744656hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38108983
hg19108983
hg18108983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563040
Samples
Known GenesLOC100131655, ZNF236
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056690
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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