A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620115



Internal ID7006988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26707654..26788040hg38UCSC Ensembl
Innerchr9:26707657..26788037hg38UCSC Ensembl
Outerchr9:26707651..26788043hg38UCSC Ensembl
chr9:26707652..26788038hg19UCSC Ensembl
Innerchr9:26707655..26788035hg19UCSC Ensembl
Outerchr9:26707649..26788041hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3880387
hg1980387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13433572, essv13433570, essv13433571
SamplesHG00443, HG00557, HG00707
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620115
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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