A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5860274



Internal ID8837677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56917940..56918245hg38UCSC Ensembl
chr4:57784106..57784411hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2663344
Supporting Variants
SamplesNA19382
Known GenesREST
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5860274
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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