A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6445984



Internal ID8954509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59729638..59773254hg38UCSC Ensembl
chr8:60642197..60685813hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3843617
hg1943617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665469
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6445984
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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