A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523068



Internal ID15103675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:4285070..4292011hg38UCSC Ensembl
Innerchr18:4285070..4292011hg19UCSC Ensembl
Innerchr18:4275070..4282011hg18UCSC Ensembl
Innerchr18:4275070..4282011hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg386942
hg196942
hg186942
hg176942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698755
Samples
Known GenesDLGAP1, DLGAP1-AS5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523068
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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