A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893965



Internal ID19184819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:80107182..80154046hg38UCSC Ensembl
Outerchr4:80107182..80154046hg38UCSC Ensembl
Innerchr4:81028336..81075200hg19UCSC Ensembl
Outerchr4:81028336..81075200hg19UCSC Ensembl
Innerchr4:81247360..81294224hg18UCSC Ensembl
Outerchr4:81247360..81294224hg18UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3846865
hg1946865
hg1846865
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788505
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893965
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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