A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676395



Internal ID9942500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108686058..108687784hg38UCSC Ensembl
chr4:109607214..109608940hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381727
hg191727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5793902, essv6109404
SamplesNA20808, HG00637
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676395
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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