A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016612



Internal ID18759147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:155474369..155495081hg38UCSC Ensembl
Innerchr5:154853929..154874641hg19UCSC Ensembl
Innerchr5:154834122..154854834hg18UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3820713
hg1920713
hg1820713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5821n100
Supporting Variantsnssv3648203
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)nsv1016612
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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