A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516490



Internal ID15097097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3448764..3451764hg38UCSC Ensembl
Innerchr18:3448762..3451762hg19UCSC Ensembl
Innerchr18:3438762..3441762hg18UCSC Ensembl
Innerchr18:3438762..3441762hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg383001
hg193001
hg183001
hg173001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv668672, nssv663700
Samples
Known GenesTGIF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516490
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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