A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689641



Internal ID18987922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:84381431..84430514hg38UCSC Ensembl
Innerchr8:85293666..85342749hg19UCSC Ensembl
Innerchr8:85456221..85505304hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3849084
hg1949084
hg1849084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031918
Supporting Variants
Samples
Known GenesRALYL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689641
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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