A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5759671



Internal ID9297881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:80602199..80910822hg38UCSC Ensembl
Innerchr4:81523353..81831976hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg38308624
hg19308624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661892
Supporting Variants
SamplesNA12878
Known GenesC4orf22
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5759671
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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