A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599409



Internal ID6986457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2601611..2603620hg38UCSC Ensembl
Innerchr4:2601630..2603602hg38UCSC Ensembl
Outerchr4:2601593..2603639hg38UCSC Ensembl
chr4:2603338..2605347hg19UCSC Ensembl
Innerchr4:2603357..2605329hg19UCSC Ensembl
Outerchr4:2603320..2605366hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg382010
hg192010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11317182
SamplesHG02090
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599409
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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