A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611733



Internal ID6651951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170307545..170312411hg38UCSC Ensembl
Innerchr6:170307579..170312377hg38UCSC Ensembl
Outerchr6:170307511..170312445hg38UCSC Ensembl
chr6:170616633..170621499hg19UCSC Ensembl
Innerchr6:170616667..170621465hg19UCSC Ensembl
Outerchr6:170616599..170621533hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg384867
hg194867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12653379
SamplesNA21127
Known GenesFAM120B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611733
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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