A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033493



Internal ID18776026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:155474295..155496521hg38UCSC Ensembl
Innerchr5:154853855..154876081hg19UCSC Ensembl
Innerchr5:154834048..154856274hg18UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3822227
hg1922227
hg1822227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5821n100
Supporting Variantsnssv3648197, nssv3648199, nssv3648198
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)nsv1033493
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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