A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023430



Internal ID19112647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8271189..8291192hg38UCSC Ensembl
Innerchr5:8271302..8291305hg19UCSC Ensembl
Innerchr5:8324302..8344305hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3820004
hg1920004
hg1820004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639649, nssv3639647, nssv3639648
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)nsv1023430
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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