A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034115



Internal ID18776649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:6689463..6808311hg38UCSC Ensembl
Innerchr8:6546984..6665832hg19UCSC Ensembl
Innerchr8:6534392..6653242hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38118849
hg19118849
hg18118851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6876n100
Supporting Variantsnssv3677433
Samples
Known GenesAGPAT5, MIR4659A, MIR4659B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034115
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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