A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022347



Internal ID19111565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8702410..8749607hg38UCSC Ensembl
Innerchr5:8702522..8749719hg19UCSC Ensembl
Innerchr5:8755522..8802719hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3847198
hg1947198
hg1847198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5564n100
Supporting Variantsnssv3746408, nssv3636711
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)nsv1022347
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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