A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5790226



Internal ID9616027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44016273..44025188hg38UCSC Ensembl
chr4:44018290..44027205hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg388916
hg198916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656939
Supporting Variants
SamplesNA19318
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5790226
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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