A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894077



Internal ID19184931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:177534370..178089493hg38UCSC Ensembl
Outerchr4:177534370..178089493hg38UCSC Ensembl
Innerchr4:178455524..179010647hg19UCSC Ensembl
Outerchr4:178455524..179010647hg19UCSC Ensembl
Innerchr4:178692518..179247641hg18UCSC Ensembl
Outerchr4:178692518..179247641hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38555124
hg19555124
hg18555124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780890
Samples
Known GenesLINC01098, LINC01099
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894077
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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