A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13559245



Internal ID3561061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91801051..91803844hg38UCSC Ensembl
Innerchr9:91801051..91803844hg38UCSC Ensembl
Outerchr9:91800834..91804071hg38UCSC Ensembl
chr9:94563333..94566126hg19UCSC Ensembl
Innerchr9:94563333..94566126hg19UCSC Ensembl
Outerchr9:94563116..94566353hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg382794
hg192794
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621071
Supporting Variants
SamplesNA19099
Known GenesROR2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13559245
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