A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600707



Internal ID6987747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62579966..62605490hg38UCSC Ensembl
Innerchr4:62579966..62605490hg38UCSC Ensembl
Outerchr4:62579466..62605990hg38UCSC Ensembl
chr4:63445684..63471208hg19UCSC Ensembl
Innerchr4:63445684..63471208hg19UCSC Ensembl
Outerchr4:63445184..63471708hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3825525
hg1925525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11457297, essv11457299, essv11457296, essv11457298
SamplesHG03800, HG03687, NA21112, NA21143
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600707
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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