A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027067



Internal ID19116286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:149688364..149725530hg38UCSC Ensembl
Innerchr5:149067927..149105093hg19UCSC Ensembl
Innerchr5:149048120..149085286hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3837167
hg1937167
hg1837167
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648163
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)nsv1027067
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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