A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3757375



Internal ID19055656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131443328..131566810hg38UCSC Ensembl
Innerchr8:132455575..132579057hg19UCSC Ensembl
Innerchr8:132524757..132648239hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38123483
hg19123483
hg18123483
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015343
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3757375
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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