A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059761



Internal ID19148980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:39360269..39456067hg38UCSC Ensembl
Innerchr18:36940233..37036031hg19UCSC Ensembl
Innerchr18:35194231..35290029hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3895799
hg1995799
hg1895799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3337n100
Supporting Variantsnssv3564218
Samples
Known GenesLINC00669
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059761
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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