A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521948



Internal ID15449241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78902714..78908622hg38UCSC Ensembl
Innerchr18:76662714..76668622hg19UCSC Ensembl
Innerchr18:74763702..74769610hg18UCSC Ensembl
Innerchr18:74763702..74769610hg17UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg385909
hg195909
hg185909
hg175909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694717
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521948
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer