A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12456322



Internal ID2458138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:86975965..86978404hg38UCSC Ensembl
Innerchr6:86975998..86978371hg38UCSC Ensembl
Outerchr6:86975932..86978437hg38UCSC Ensembl
chr6:87685683..87688122hg19UCSC Ensembl
Innerchr6:87685716..87688089hg19UCSC Ensembl
Outerchr6:87685650..87688155hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg382440
hg192440
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609856
Supporting Variants
SamplesNA20878
Known GenesHTR1E
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12456322
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