A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483121



Internal ID15235595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85023159..85193909hg38UCSC Ensembl
Innerchr8:85935394..86106144hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38170751
hg19170751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996018
Samples
Known GenesE2F5, LRRCC1
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483121
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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