A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033825



Internal ID19123046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:163318463..163378839hg38UCSC Ensembl
Innerchr5:162745469..162805845hg19UCSC Ensembl
Innerchr5:162678047..162738423hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3860377
hg1960377
hg1860377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5826n100
Supporting Variantsnssv3746662, nssv3746661
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)nsv1033825
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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