A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022838



Internal ID19112056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:27324114..27411181hg38UCSC Ensembl
Innerchr5:27324221..27411288hg19UCSC Ensembl
Innerchr5:27359978..27447045hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3887068
hg1987068
hg1887068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5610n100
Supporting Variantsnssv3745862
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)nsv1022838
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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