A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621780



Internal ID6661956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127347381..127347959hg38UCSC Ensembl
Innerchr9:127347382..127347958hg38UCSC Ensembl
Outerchr9:127347380..127347960hg38UCSC Ensembl
chr9:130109660..130110238hg19UCSC Ensembl
Innerchr9:130109661..130110237hg19UCSC Ensembl
Outerchr9:130109659..130110239hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13621953, essv13621954, essv13621947, essv13621950, essv13621945, essv13621952, essv13621951, essv13621946, essv13621949, essv13621948
SamplesHG02657, HG03900, NA21125, HG03729, HG03940, HG04100, NA20875, NA21115, NA20884, HG03702
Known GenesGARNL3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621780
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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