A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621475



Internal ID6661654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110896895..110926031hg38UCSC Ensembl
Innerchr9:110896977..110925949hg38UCSC Ensembl
Outerchr9:110896813..110926113hg38UCSC Ensembl
chr9:113659175..113688311hg19UCSC Ensembl
Innerchr9:113659257..113688229hg19UCSC Ensembl
Outerchr9:113659093..113688393hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3829137
hg1929137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13601047
SamplesHG00533
Known GenesLPAR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621475
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