A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3760499



Internal ID19058780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25757187..25787720hg38UCSC Ensembl
Innerchr8:25614703..25645236hg19UCSC Ensembl
Innerchr8:25670620..25701153hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3830534
hg1930534
hg1830534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018451
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3760499
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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