A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3677433



Internal ID18629028
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 StatusS
Merged Variantsnsv1034115
Supporting Variants
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)nssv3677433
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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