A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015565



Internal ID18758099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133995284..134147172hg38UCSC Ensembl
Innerchr4:134916439..135068327hg19UCSC Ensembl
Innerchr4:135135889..135287777hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38151889
hg19151889
hg18151889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639537
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)nsv1015565
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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