A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019978



Internal ID19109197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:152898460..152936886hg38UCSC Ensembl
Innerchr5:152278020..152316446hg19UCSC Ensembl
Innerchr5:152258213..152296639hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3838427
hg1938427
hg1838427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648185, nssv3648186
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)nsv1019978
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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