A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6374683



Internal ID9099600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110847352..110848350hg38UCSC Ensembl
chr6:111168555..111169553hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38999
hg19999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2677721
Supporting Variants
SamplesHG01082
Known GenesAMD1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6374683
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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