A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5940062



Internal ID8917465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:85650144..85651757hg38UCSC Ensembl
chr4:86571297..86572910hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg381614
hg191614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670543
Supporting Variants
SamplesNA19701
Known GenesARHGAP24
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5940062
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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