A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656836



Internal ID9922941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151970295..151972528hg38UCSC Ensembl
chr4:152891447..152893680hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382234
hg192234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6368204, essv6501863, essv5670509, essv6178150, essv6375958, essv6575433, essv6178933
SamplesNA19684, HG00236, HG00734, NA20516, HG00343, HG00252, HG00345
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656836
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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