A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019344



Internal ID19108562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:114600122..114685855hg38UCSC Ensembl
Innerchr5:113935819..114021552hg19UCSC Ensembl
Innerchr5:113963718..114049451hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3885734
hg1985734
hg1885734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5786n100
Supporting Variantsnssv3746586
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)nsv1019344
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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