A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599652



Internal ID6986697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11624709..11858769hg38UCSC Ensembl
Innerchr4:11624709..11858769hg38UCSC Ensembl
Outerchr4:11624209..11859269hg38UCSC Ensembl
chr4:11626333..11860393hg19UCSC Ensembl
Innerchr4:11626333..11860393hg19UCSC Ensembl
Outerchr4:11625833..11860893hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38234061
hg19234061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv985e214
Supporting Variantsessv11357081
SamplesHG04080
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599652
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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