A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6178933



Internal ID8893812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151970295..151972528hg38UCSC Ensembl
chr4:152891447..152893680hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382234
hg192234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656836
Supporting Variants
SamplesHG00343
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6178933
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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