A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057907



Internal ID19147126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:67944783..68114725hg38UCSC Ensembl
Innerchr18:65612020..65781962hg19UCSC Ensembl
Innerchr18:63763000..63932942hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38169943
hg19169943
hg18169943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3389n100
Supporting Variantsnssv3566452
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)nsv1057907
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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