A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599891



Internal ID6986936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22051172..22070603hg38UCSC Ensembl
chr4:22052795..22072226hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3819432
hg1919432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv994e214
Supporting Variantsessv11369855, essv11369851, essv11369852, essv11369854, essv11369853
SamplesHG01521, NA20891, NA12400, NA07357, NA20900
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599891
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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