A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518334



Internal ID15445627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9994688..10132919hg38UCSC Ensembl
Innerchr18:9994685..10132916hg19UCSC Ensembl
Innerchr18:9984685..10122916hg18UCSC Ensembl
Innerchr18:9984685..10122916hg17UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38138232
hg19138232
hg18138232
hg17138232
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695763
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518334
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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