A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6115416



Internal ID9118180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119641627..119698044hg38UCSC Ensembl
chr6:119962788..120019201hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3856418
hg1956414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668839
Supporting Variants
SamplesHG01125
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6115416
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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