A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996018



Internal ID15234878
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 Flag1
Merged StatusS
Merged Variantsnsv483121
Supporting Variants
Samples
Known GenesE2F5, LRRCC1
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996018
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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