A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893974



Internal ID18838142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:85829546..85842748hg38UCSC Ensembl
Outerchr4:85829546..85842748hg38UCSC Ensembl
Innerchr4:86750699..86763901hg19UCSC Ensembl
Outerchr4:86750699..86763901hg19UCSC Ensembl
Innerchr4:86969723..86982925hg18UCSC Ensembl
Outerchr4:86969723..86982925hg18UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3813203
hg1913203
hg1813203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781707
Samples
Known GenesARHGAP24
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893974
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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