A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890731



Internal ID19185033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:122233974..122278005hg38UCSC Ensembl
Outerchr5:122233974..122278005hg38UCSC Ensembl
Innerchr5:121569669..121613700hg19UCSC Ensembl
Outerchr5:121569669..121613700hg19UCSC Ensembl
Innerchr5:121597568..121641599hg18UCSC Ensembl
Outerchr5:121597568..121641599hg18UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3844032
hg1944032
hg1844032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785856
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890731
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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