A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6544431



Internal ID9066558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33644054..33672967hg38UCSC Ensembl
chr8:33501572..33530485hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3828914
hg1928914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669648
Supporting Variants
SamplesHG00734
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6544431
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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