A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12457756



Internal ID5093261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89091676..89093011hg38UCSC Ensembl
Innerchr6:89091676..89093011hg38UCSC Ensembl
Outerchr6:89091461..89093230hg38UCSC Ensembl
chr6:89801395..89802730hg19UCSC Ensembl
Innerchr6:89801395..89802730hg19UCSC Ensembl
Outerchr6:89801180..89802949hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381336
hg191336
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609895
Supporting Variants
SamplesNA18549
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12457756
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