A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6440602



Internal ID9418005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160206718..160217064hg38UCSC Ensembl
chr6:160627750..160638096hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3810347
hg1910347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660610
Supporting Variants
SamplesNA19404
Known GenesSLC22A2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6440602
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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