A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12622207



Internal ID4171408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162820384..162898837hg38UCSC Ensembl
Innerchr6:162820384..162898837hg38UCSC Ensembl
Outerchr6:162819884..162899337hg38UCSC Ensembl
chr6:163241416..163319869hg19UCSC Ensembl
Innerchr6:163241416..163319869hg19UCSC Ensembl
Outerchr6:163240916..163320369hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3878454
hg1978454
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611568
Supporting Variants
SamplesHG03772
Known GenesPACRG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12622207
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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