A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607916



Internal ID6994847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2843530..2846182hg38UCSC Ensembl
Innerchr6:2843533..2846179hg38UCSC Ensembl
Outerchr6:2843527..2846185hg38UCSC Ensembl
chr6:2843764..2846416hg19UCSC Ensembl
Innerchr6:2843767..2846413hg19UCSC Ensembl
Outerchr6:2843761..2846419hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382653
hg192653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12177683
SamplesHG03303
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607916
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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