A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv26e214



Internal ID22755920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:72545350..72629194hg38UCSC Ensembl
chr1:73011033..73094877hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3883845
hg1983845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3586417, esv3586418
SamplesHG00244, NA12889, HG03973
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv26e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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