A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030395



Internal ID19119614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:35446414..35491083hg38UCSC Ensembl
Innerchr5:35446516..35491185hg19UCSC Ensembl
Innerchr5:35482273..35526942hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3844670
hg1944670
hg1844670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5630n100
Supporting Variantsnssv3637070
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)nsv1030395
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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