A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663344



Internal ID9582763
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 StatusM
Merged Variants
Supporting Variantsessv6554678, essv6403036, essv5860274, essv6357520
SamplesNA19359, NA19396, NA19382, NA19391
Known GenesREST
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663344
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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