A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890654



Internal ID18838052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:71057176..71083639hg38UCSC Ensembl
Outerchr5:71057176..71083639hg38UCSC Ensembl
Innerchr5:70353003..70379466hg19UCSC Ensembl
Outerchr5:70353003..70379466hg19UCSC Ensembl
Innerchr5:70388759..70415222hg18UCSC Ensembl
Outerchr5:70388759..70415222hg18UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3826464
hg1926464
hg1826464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782644
Samples
Known GenesGTF2H2, GTF2H2B, GTF2H2C, GTF2H2D, LOC647859
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890654
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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