A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5955925



Internal ID9558654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:183184888..183185125hg38UCSC Ensembl
Outerchr4:183184851..183185175hg38UCSC Ensembl
Innerchr4:184106041..184106278hg19UCSC Ensembl
Outerchr4:184106004..184106328hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2671317
Supporting Variants
SamplesNA19093
Known GenesWWC2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5955925
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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