A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11733340



Internal ID4757014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184236838..184247976hg38UCSC Ensembl
Innerchr4:184236854..184247960hg38UCSC Ensembl
Outerchr4:184236822..184247992hg38UCSC Ensembl
chr4:185157991..185169129hg19UCSC Ensembl
Innerchr4:185158007..185169113hg19UCSC Ensembl
Outerchr4:185157975..185169145hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3811139
hg1911139
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603455
Supporting Variants
SamplesNA10851
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11733340
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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