A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026174



Internal ID18768706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:83955411..83987123hg38UCSC Ensembl
Innerchr5:83251230..83282942hg19UCSC Ensembl
Innerchr5:83286986..83318698hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3831713
hg1931713
hg1831713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5709n100
Supporting Variantsnssv3639150
Samples
Known GenesEDIL3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026174
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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