A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603358



Internal ID6990390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:179666105..179708690hg38UCSC Ensembl
Innerchr4:179666105..179708690hg38UCSC Ensembl
Outerchr4:179665605..179709190hg38UCSC Ensembl
chr4:180587258..180629843hg19UCSC Ensembl
Innerchr4:180587258..180629843hg19UCSC Ensembl
Outerchr4:180586758..180630343hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3842586
hg1942586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11727315
SamplesHG02165
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603358
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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