A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600655



Internal ID6987696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:59843490..59892343hg38UCSC Ensembl
Innerchr4:59843518..59892316hg38UCSC Ensembl
Outerchr4:59843463..59892371hg38UCSC Ensembl
chr4:60709208..60758061hg19UCSC Ensembl
Innerchr4:60709236..60758034hg19UCSC Ensembl
Outerchr4:60709181..60758089hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3848854
hg1948854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11446011
SamplesNA18531
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600655
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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