A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027685



Internal ID18770217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:1588960..1665298hg38UCSC Ensembl
Innerchr8:1537126..1613464hg19UCSC Ensembl
Innerchr8:1524533..1600871hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3876339
hg1976339
hg1876339
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6803n100
Supporting Variantsnssv3675053, nssv3675052
Samples
Known GenesDLGAP2, LOC100507435
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027685
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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