A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996211



Internal ID15581712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:32308555..32460333hg38UCSC Ensembl
Innerchr18:29888518..30040296hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38151779
hg19151779
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv482915
Supporting Variants
Samples
Known GenesGAREM
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996211
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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