A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621972



Internal ID7008838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134994145..134994721hg38UCSC Ensembl
Innerchr9:134994151..134994715hg38UCSC Ensembl
Outerchr9:134994139..134994727hg38UCSC Ensembl
chr9:137885991..137886567hg19UCSC Ensembl
Innerchr9:137885997..137886561hg19UCSC Ensembl
Outerchr9:137885985..137886573hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13648197, essv13648198, essv13648194, essv13648199, essv13648195, essv13648196, essv13648193
SamplesHG03577, HG02715, HG03547, HG03382, HG02304, HG02839, HG03025
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621972
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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