A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608370



Internal ID6995300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24748787..24758894hg38UCSC Ensembl
Innerchr6:24748837..24758844hg38UCSC Ensembl
Outerchr6:24748737..24758944hg38UCSC Ensembl
chr6:24749015..24759122hg19UCSC Ensembl
Innerchr6:24749065..24759072hg19UCSC Ensembl
Outerchr6:24748965..24759172hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3810108
hg1910108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12229666
SamplesHG03069
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608370
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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