A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027297



Internal ID19116516
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 StatusM
Merged Variantsdgv7228n100
Supporting Variantsnssv3688678, nssv3688679
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)nsv1027297
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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