A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13404372



Internal ID1030691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:12008134..12121467hg38UCSC Ensembl
Innerchr9:12008634..12120967hg38UCSC Ensembl
Outerchr9:12007134..12122467hg38UCSC Ensembl
chr9:12008134..12121467hg19UCSC Ensembl
Innerchr9:12008634..12120967hg19UCSC Ensembl
Outerchr9:12007134..12122467hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38113334
hg19113334
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619665
Supporting Variants
SamplesHG00651
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13404372
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