A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689676



Internal ID18641271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:86155561..86322968hg38UCSC Ensembl
Innerchr8:87167790..87335197hg19UCSC Ensembl
Innerchr8:87236906..87404313hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38167408
hg19167408
hg18167408
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016050
Supporting Variants
Samples
Known GenesSLC7A13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689676
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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