A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13602699



Internal ID3604515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111588707..111589877hg38UCSC Ensembl
Innerchr9:111588707..111589877hg38UCSC Ensembl
Outerchr9:111588521..111589989hg38UCSC Ensembl
chr9:114350987..114352157hg19UCSC Ensembl
Innerchr9:114350987..114352157hg19UCSC Ensembl
Outerchr9:114350801..114352269hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381171
hg191171
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621494
Supporting Variants
SamplesNA18988
Known GenesPTGR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13602699
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