A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746540



Internal ID19044821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:106609054..106670812hg38UCSC Ensembl
Innerchr5:105944755..106006513hg19UCSC Ensembl
Innerchr5:105972654..106034412hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3861759
hg1961759
hg1861759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022395
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)nssv3746540
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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