A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599660



Internal ID6986705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11878633..11897172hg38UCSC Ensembl
Innerchr4:11879133..11896672hg38UCSC Ensembl
Outerchr4:11877633..11898172hg38UCSC Ensembl
chr4:11880257..11898796hg19UCSC Ensembl
Innerchr4:11880757..11898296hg19UCSC Ensembl
Outerchr4:11879257..11899796hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3818540
hg1918540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11357239, essv11357238, essv11357240
SamplesHG03645, HG04080, HG01781
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599660
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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