A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5923878



Internal ID9676003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52763797..52804145hg38UCSC Ensembl
chr6:52628595..52668943hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3840349
hg1940349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666921
Supporting Variants
SamplesNA19404
Known GenesGSTA1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5923878
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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