A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5396037



Internal ID8373440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167129527..167130932hg38UCSC Ensembl
chr6:167543015..167544420hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381406
hg191406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664671
Supporting Variants
SamplesNA18910
Known GenesCCR6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5396037
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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