A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5577534



Internal ID9699175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70889294..70891972hg38UCSC Ensembl
chr6:71598997..71601675hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg382679
hg192679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676925
Supporting Variants
SamplesNA19449
Known GenesB3GAT2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5577534
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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