A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5644496



Internal ID8621899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109919582..109924580hg38UCSC Ensembl
chr4:110840738..110845736hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg384999
hg194999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672203
Supporting Variants
SamplesNA19430
Known GenesEGF
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5644496
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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