A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620323



Internal ID7007194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33417850..33420940hg38UCSC Ensembl
Innerchr9:33417850..33420940hg38UCSC Ensembl
Outerchr9:33417586..33421223hg38UCSC Ensembl
chr9:33417848..33420938hg19UCSC Ensembl
Innerchr9:33417848..33420938hg19UCSC Ensembl
Outerchr9:33417584..33421221hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg383091
hg193091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13456343, essv13456345, essv13456342, essv13456346, essv13456344
SamplesHG02727, HG02792, HG02737, HG02789, HG03488
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620323
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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