A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13447262



Internal ID1366275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:31414252..31440180hg38UCSC Ensembl
Innerchr9:31414288..31440144hg38UCSC Ensembl
Outerchr9:31414216..31440216hg38UCSC Ensembl
chr9:31414250..31440178hg19UCSC Ensembl
Innerchr9:31414286..31440142hg19UCSC Ensembl
Outerchr9:31414214..31440214hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3825929
hg1925929
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620277
Supporting Variants
SamplesHG01205
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13447262
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