A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689665



Internal ID18987946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85823138..85866941hg38UCSC Ensembl
Innerchr8:86835367..86879170hg19UCSC Ensembl
Innerchr8:86904661..86948287hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3843804
hg1943804
hg1843627
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023182
Supporting Variants
Samples
Known GenesREXO1L2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689665
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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