A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033167



Internal ID19122389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:6972112..7189812hg38UCSC Ensembl
Innerchr5:6972225..7189925hg19UCSC Ensembl
Innerchr5:7025225..7242925hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38217701
hg19217701
hg18217701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638601
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)nsv1033167
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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