A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5459081



Internal ID8436484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:3070474..3072561hg38UCSC Ensembl
Outerchr6:3070317..3072714hg38UCSC Ensembl
Innerchr6:3070708..3072795hg19UCSC Ensembl
Outerchr6:3070551..3072948hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382398
hg192398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663461
Supporting Variants
SamplesNA18605
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5459081
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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