A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996526



Internal ID15235386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32882976..33031504hg38UCSC Ensembl
Innerchr6:32850753..32999281hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38148529
hg19148529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483081
Supporting Variants
Samples
Known GenesBRD2, HLA-DMA, HLA-DMB, HLA-DOA, LOC100294145
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996526
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