A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027842



Internal ID19117060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:121381995..121415103hg38UCSC Ensembl
Innerchr8:122394235..122427343hg19UCSC Ensembl
Innerchr8:122463416..122496524hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3833109
hg1933109
hg1833109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691481
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)nsv1027842
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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