A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3757319



Internal ID19055600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:87448384..87567538hg38UCSC Ensembl
Innerchr8:88460612..88579766hg19UCSC Ensembl
Innerchr8:88529728..88648882hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38119155
hg19119155
hg18119155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025811
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)nssv3757319
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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