A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3681629



Internal ID18979910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8120476..8283909hg38UCSC Ensembl
Innerchr8:7977998..8141431hg19UCSC Ensembl
Innerchr8:8015408..8178841hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38163434
hg19163434
hg18163434
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026278
Supporting Variants
Samples
Known GenesFAM86B3P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3681629
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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