A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586835



Internal ID6627144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94220845..94224954hg38UCSC Ensembl
Innerchr1:94220857..94224942hg38UCSC Ensembl
Outerchr1:94220833..94224966hg38UCSC Ensembl
chr1:94686401..94690510hg19UCSC Ensembl
Innerchr1:94686413..94690498hg19UCSC Ensembl
Outerchr1:94686389..94690522hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg384110
hg194110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10023700
SamplesHG01705
Known GenesARHGAP29
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586835
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