A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017238



Internal ID18759773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8902628..8974152hg38UCSC Ensembl
Innerchr8:8760138..8831662hg19UCSC Ensembl
Innerchr8:8797548..8869072hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3871525
hg1971525
hg1871525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3681695
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)nsv1017238
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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