A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022253



Internal ID19111471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29076353..29195880hg38UCSC Ensembl
Innerchr5:29076460..29195987hg19UCSC Ensembl
Innerchr5:29112217..29231744hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38119528
hg19119528
hg18119528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745863
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)nsv1022253
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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