A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061135



Internal ID19150354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1905345..1980033hg38UCSC Ensembl
Innerchr18:1905346..1980034hg19UCSC Ensembl
Innerchr18:1895346..1970034hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3874689
hg1974689
hg1874689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3311n100
Supporting Variantsnssv3563963
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061135
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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