A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13596444



Internal ID2588303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109553749..109565123hg38UCSC Ensembl
Innerchr9:109553749..109565123hg38UCSC Ensembl
Outerchr9:109553528..109565325hg38UCSC Ensembl
chr9:112316029..112327403hg19UCSC Ensembl
Innerchr9:112316029..112327403hg19UCSC Ensembl
Outerchr9:112315808..112327605hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3811375
hg1911375
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621437
Supporting Variants
SamplesHG02291
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13596444
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