A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893924



Internal ID19184778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:58342013..58740459hg38UCSC Ensembl
Outerchr4:58342013..58740459hg38UCSC Ensembl
Innerchr4:59208179..59606624hg19UCSC Ensembl
Outerchr4:59208179..59606624hg19UCSC Ensembl
Innerchr4:58902936..59301381hg18UCSC Ensembl
Outerchr4:58902936..59301381hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38398447
hg19398446
hg18398446
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799831
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893924
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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