A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608153



Internal ID6995083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14770593..14781346hg38UCSC Ensembl
Innerchr6:14770593..14781346hg38UCSC Ensembl
Outerchr6:14770093..14781846hg38UCSC Ensembl
chr6:14770824..14781577hg19UCSC Ensembl
Innerchr6:14770824..14781577hg19UCSC Ensembl
Outerchr6:14770324..14782077hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3810754
hg1910754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12199763
SamplesHG02970
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608153
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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