A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659603



Internal ID9925708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119210350..119211834hg38UCSC Ensembl
chr4:120131505..120132989hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg381485
hg191485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6365533, essv5539751, essv5488493, essv6483557, essv5870377, essv5505564
SamplesHG00427, HG00657, HG00533, NA18630, HG00611, HG00437
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659603
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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