A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7527395



Internal ID10458991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109683378..109699378hg38UCSC Ensembl
Innerchr1:110226000..110242000hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3816001
hg1916001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3257828
Supporting Variants
SamplesHuRef
Known GenesGSTM1, GSTM2
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7527395
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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