A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5564455



Internal ID9600270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88601757..88602072hg38UCSC Ensembl
chr4:89522908..89523223hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2657218
Supporting Variants
SamplesNA19238
Known GenesHERC3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5564455
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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