A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5444170



Internal ID9810510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186292826..186293603hg38UCSC Ensembl
chr4:187213980..187214757hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38778
hg19778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2677779
Supporting Variants
SamplesNA19916
Known GenesF11-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5444170
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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