A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6095150



Internal ID8916401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:45646209..45646707hg38UCSC Ensembl
Outerchr6:45646172..45646757hg38UCSC Ensembl
Innerchr6:45613946..45614444hg19UCSC Ensembl
Outerchr6:45613909..45614494hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2657263
Supporting Variants
SamplesHG00418
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6095150
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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