A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603442



Internal ID6990473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183562968..183566954hg38UCSC Ensembl
Innerchr4:183562968..183566954hg38UCSC Ensembl
Outerchr4:183562750..183567162hg38UCSC Ensembl
chr4:184484121..184488107hg19UCSC Ensembl
Innerchr4:184484121..184488107hg19UCSC Ensembl
Outerchr4:184483903..184488315hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg383987
hg193987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11732424
SamplesNA19440
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603442
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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