A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608276



Internal ID6995206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19564751..19572484hg38UCSC Ensembl
Innerchr6:19564752..19572483hg38UCSC Ensembl
Outerchr6:19564750..19572485hg38UCSC Ensembl
chr6:19564982..19572715hg19UCSC Ensembl
Innerchr6:19564983..19572714hg19UCSC Ensembl
Outerchr6:19564981..19572716hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg387734
hg197734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12214123
SamplesHG02721
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608276
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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