A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685511



Internal ID18983792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25757187..25788663hg38UCSC Ensembl
Innerchr8:25614703..25646179hg19UCSC Ensembl
Innerchr8:25670620..25702096hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3831477
hg1931477
hg1831477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015150
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)nssv3685511
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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