A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12668869



Internal ID2123116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2901945..2905840hg38UCSC Ensembl
Innerchr7:2901995..2905790hg38UCSC Ensembl
Outerchr7:2901895..2905890hg38UCSC Ensembl
chr7:2941579..2945474hg19UCSC Ensembl
Innerchr7:2941629..2945424hg19UCSC Ensembl
Outerchr7:2941529..2945524hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg383896
hg193896
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611857
Supporting Variants
SamplesHG01927
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12668869
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