A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3687492



Internal ID18639087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:51576279..51606163hg38UCSC Ensembl
Innerchr8:52488839..52518723hg19UCSC Ensembl
Innerchr8:52651392..52681276hg18UCSC Ensembl
Cytoband8q11.22
Allele length
AssemblyAllele length
hg3829885
hg1929885
hg1829885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021919
Supporting Variants
Samples
Known GenesPXDNL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3687492
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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