A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057808



Internal ID18800339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:766118..803577hg38UCSC Ensembl
Innerchr18:766119..803578hg19UCSC Ensembl
Innerchr18:756119..793578hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3837460
hg1937460
hg1837460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563894
Samples
Known GenesYES1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057808
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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