A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3675047



Internal ID18626642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:1588960..1635474hg38UCSC Ensembl
Innerchr8:1537126..1583640hg19UCSC Ensembl
Innerchr8:1524533..1571047hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3846515
hg1946515
hg1846515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026633
Supporting Variants
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)nssv3675047
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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