A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6310999



Internal ID9098110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33956866..33974730hg38UCSC Ensembl
chr6:33924643..33942507hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3817865
hg1917865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658092
Supporting Variants
SamplesHG01080
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6310999
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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