A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034899



Internal ID19124119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131665346..131692919hg38UCSC Ensembl
Innerchr8:132677593..132705166hg19UCSC Ensembl
Innerchr8:132746775..132774348hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3827574
hg1927574
hg1827574
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7314n100
Supporting Variantsnssv3691533
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)nsv1034899
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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