A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585150



Internal ID6972674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8705848..8715317hg38UCSC Ensembl
Innerchr1:8705848..8715317hg38UCSC Ensembl
Outerchr1:8705752..8715485hg38UCSC Ensembl
chr1:8765907..8775376hg19UCSC Ensembl
Innerchr1:8765907..8775376hg19UCSC Ensembl
Outerchr1:8765811..8775544hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg389470
hg199470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9849705
SamplesNA18508
Known GenesRERE
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585150
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