A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6056287



Internal ID9033690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83546228..83547495hg38UCSC Ensembl
chr4:84467381..84468648hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg381268
hg191268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676861
Supporting Variants
SamplesHG01079
Known GenesAGPAT9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6056287
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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