A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12594589



Internal ID1252385
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611331
Supporting Variants
SamplesHG01105
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12594589
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer