A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6164993



Internal ID9142396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:30918653..30918793hg38UCSC Ensembl
chr6:30886430..30886570hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2677874
Supporting Variants
SamplesNA12154
Known GenesVARS2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6164993
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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