A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611331



Internal ID6998240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154852175..154853472hg38UCSC Ensembl
Innerchr6:154852221..154853426hg38UCSC Ensembl
Outerchr6:154852129..154853518hg38UCSC Ensembl
chr6:155173309..155174606hg19UCSC Ensembl
Innerchr6:155173355..155174560hg19UCSC Ensembl
Outerchr6:155173263..155174652hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg381298
hg191298
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12594589
SamplesHG01105
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611331
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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