A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608001



Internal ID6994932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6898164..6905344hg38UCSC Ensembl
Innerchr6:6898164..6905344hg38UCSC Ensembl
Outerchr6:6897974..6905459hg38UCSC Ensembl
chr6:6898397..6905577hg19UCSC Ensembl
Innerchr6:6898397..6905577hg19UCSC Ensembl
Outerchr6:6898207..6905692hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg387181
hg197181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12182911, essv12182910
SamplesHG03817, NA18977
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608001
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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