A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027038



Internal ID19116257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:35503785..35556145hg38UCSC Ensembl
Innerchr5:35503887..35556247hg19UCSC Ensembl
Innerchr5:35539644..35592004hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3852361
hg1952361
hg1852361
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3637071
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)nsv1027038
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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