A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13581232



Internal ID1280042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100910171..100920104hg38UCSC Ensembl
Innerchr9:100910171..100920104hg38UCSC Ensembl
Outerchr9:100910001..100920290hg38UCSC Ensembl
chr9:103672453..103682386hg19UCSC Ensembl
Innerchr9:103672453..103682386hg19UCSC Ensembl
Outerchr9:103672283..103682572hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg389934
hg199934
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621241
Supporting Variants
SamplesHG01125
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13581232
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