A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688707



Internal ID18986988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:57165988..57248880hg38UCSC Ensembl
Innerchr8:58078547..58161439hg19UCSC Ensembl
Innerchr8:58241101..58323993hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3882893
hg1982893
hg1882893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034068
Supporting Variants
Samples
Known GenesLOC100507651
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3688707
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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