A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6362603



Internal ID9351944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158745097..158753965hg38UCSC Ensembl
chr6:159166129..159174997hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg388869
hg198869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663267
Supporting Variants
SamplesNA18547
Known GenesSYTL3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6362603
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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