A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678919



Internal ID15068885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:86188898..86321739hg38UCSC Ensembl
Innerchr8:87201127..87333968hg19UCSC Ensembl
Innerchr8:87270243..87403084hg18UCSC Ensembl
Innerchr8:87270243..87403084hg17UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38132842
hg19132842
hg18132842
hg17132842
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519507
Supporting Variants
Samples
Known GenesSLC7A13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678919
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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