A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5641755



Internal ID8619158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52761464..52762080hg38UCSC Ensembl
chr6:52626262..52626878hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666271
Supporting Variants
SamplesHG00637
Known GenesGSTA2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5641755
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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