A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034890



Internal ID19124110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:114590082..114642262hg38UCSC Ensembl
Innerchr5:113925779..113977959hg19UCSC Ensembl
Innerchr5:113953678..114005858hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3852181
hg1952181
hg1852181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5785n100
Supporting Variantsnssv3647073
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)nsv1034890
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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