A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11540521



Internal ID3905633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:96648270..96664885hg38UCSC Ensembl
Innerchr4:96648770..96664385hg38UCSC Ensembl
Outerchr4:96647270..96665885hg38UCSC Ensembl
chr4:97569421..97586036hg19UCSC Ensembl
Innerchr4:97569921..97585536hg19UCSC Ensembl
Outerchr4:97568421..97587036hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3816616
hg1916616
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3601494
Supporting Variants
SamplesHG03559
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11540521
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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