A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611053



Internal ID6997964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:141498740..141507672hg38UCSC Ensembl
Innerchr6:141498750..141507663hg38UCSC Ensembl
Outerchr6:141498731..141507682hg38UCSC Ensembl
chr6:141819877..141828809hg19UCSC Ensembl
Innerchr6:141819887..141828800hg19UCSC Ensembl
Outerchr6:141819868..141828819hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg388933
hg198933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12573191
SamplesHG00844
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611053
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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