A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029060



Internal ID19118279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:27313724..27411181hg38UCSC Ensembl
Innerchr5:27313831..27411288hg19UCSC Ensembl
Innerchr5:27349588..27447045hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3897458
hg1997458
hg1897458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5610n100
Supporting Variantsnssv3635967
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)nsv1029060
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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