A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608191



Internal ID6995121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16218234..16222013hg38UCSC Ensembl
Innerchr6:16218247..16222001hg38UCSC Ensembl
Outerchr6:16218222..16222026hg38UCSC Ensembl
chr6:16218465..16222244hg19UCSC Ensembl
Innerchr6:16218478..16222232hg19UCSC Ensembl
Outerchr6:16218453..16222257hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383780
hg193780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12200614
SamplesHG04200
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608191
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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