A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893873



Internal ID18838007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9943026..10036488hg38UCSC Ensembl
Outerchr4:9943026..10036488hg38UCSC Ensembl
Innerchr4:9944650..10038112hg19UCSC Ensembl
Outerchr4:9944650..10038112hg19UCSC Ensembl
Innerchr4:9553748..9647210hg18UCSC Ensembl
Outerchr4:9553748..9647210hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3893463
hg1993463
hg1893463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796932
Samples
Known GenesSLC2A9
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893873
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer