A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483109



Internal ID15582222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:41621997..41786592hg38UCSC Ensembl
Innerchr18:39201961..39366557hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38164596
hg19164597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2995911
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483109
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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