A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688678



Internal ID18986959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:55806899..55964201hg38UCSC Ensembl
Innerchr8:56719458..56876760hg19UCSC Ensembl
Innerchr8:56882012..57039314hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38157303
hg19157303
hg18157303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027297
Supporting Variants
Samples
Known GenesLYN, TGS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3688678
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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