A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608147



Internal ID6995077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14585036..14587475hg38UCSC Ensembl
Innerchr6:14585036..14587475hg38UCSC Ensembl
Outerchr6:14584855..14587698hg38UCSC Ensembl
chr6:14585267..14587706hg19UCSC Ensembl
Innerchr6:14585267..14587706hg19UCSC Ensembl
Outerchr6:14585086..14587929hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg382440
hg192440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12197327
SamplesHG02076
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608147
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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