A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601794



Internal ID6988830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112028234..112074094hg38UCSC Ensembl
Innerchr4:112028248..112074081hg38UCSC Ensembl
Outerchr4:112028221..112074108hg38UCSC Ensembl
chr4:112949390..112995250hg19UCSC Ensembl
Innerchr4:112949404..112995237hg19UCSC Ensembl
Outerchr4:112949377..112995264hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3845861
hg1945861
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11565200
SamplesHG00407
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601794
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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