A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621875



Internal ID7008741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131242675..131243425hg38UCSC Ensembl
Innerchr9:131242726..131243375hg38UCSC Ensembl
Outerchr9:131242625..131243476hg38UCSC Ensembl
chr9:134118062..134118812hg19UCSC Ensembl
Innerchr9:134118113..134118762hg19UCSC Ensembl
Outerchr9:134118012..134118863hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38751
hg19751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13630768
SamplesHG02691
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621875
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