A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996284



Internal ID15235144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:27620569..27764316hg38UCSC Ensembl
Innerchr18:25200533..25344280hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38143748
hg19143748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483068
Supporting Variants
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996284
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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