A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13436357



Internal ID4680473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28132258..28467447hg38UCSC Ensembl
Innerchr9:28132267..28467439hg38UCSC Ensembl
Outerchr9:28132250..28467456hg38UCSC Ensembl
chr9:28132256..28467445hg19UCSC Ensembl
Innerchr9:28132265..28467437hg19UCSC Ensembl
Outerchr9:28132248..28467454hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38335190
hg19335190
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620149
Supporting Variants
SamplesHG04206
Known GenesLINGO2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13436357
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