A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056589



Internal ID19145808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62209749..62274023hg38UCSC Ensembl
Innerchr18:59876982..59941256hg19UCSC Ensembl
Innerchr18:58027962..58092236hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3864275
hg1964275
hg1864275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565624
Samples
Known GenesKIAA1468
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056589
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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