A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677793



Internal ID9943898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34434180..34440475hg38UCSC Ensembl
chr6:34401957..34408252hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg386296
hg196296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5623678
SamplesHG00328
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677793
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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