A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3666976



Internal ID18618571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12716562..12746900hg38UCSC Ensembl
Innerchr8:12574071..12604409hg19UCSC Ensembl
Innerchr8:12618442..12648780hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3830339
hg1930339
hg1830339
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029648
Supporting Variants
Samples
Known GenesLONRF1, MIR3926-1, MIR3926-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3666976
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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