A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893919



Internal ID19184773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:40648481..40666096hg38UCSC Ensembl
Outerchr4:40648481..40666096hg38UCSC Ensembl
Innerchr4:40650498..40668113hg19UCSC Ensembl
Outerchr4:40650498..40668113hg19UCSC Ensembl
Innerchr4:40345255..40362870hg18UCSC Ensembl
Outerchr4:40345255..40362870hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3817616
hg1917616
hg1817616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787203
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893919
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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