A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3745835



Internal ID19044116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:20886606..21325152hg38UCSC Ensembl
Innerchr5:20886715..21325261hg19UCSC Ensembl
Innerchr5:20922472..21361018hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38438547
hg19438547
hg18438547
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024176
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)nssv3745835
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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