A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5764520



Internal ID8845224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118322558..118325922hg38UCSC Ensembl
chr4:119243713..119247077hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg383365
hg193365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662314
Supporting Variants
SamplesHG00281
Known GenesPRSS12
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5764520
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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