A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3745863



Internal ID19044144
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 StatusS
Merged Variantsnsv1022253
Supporting Variants
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)nssv3745863
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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