A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13451450



Internal ID1298971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32985517..32986725hg38UCSC Ensembl
Innerchr9:32985517..32986725hg38UCSC Ensembl
Outerchr9:32985331..32986854hg38UCSC Ensembl
chr9:32985515..32986723hg19UCSC Ensembl
Innerchr9:32985515..32986723hg19UCSC Ensembl
Outerchr9:32985329..32986852hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg381209
hg191209
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620313
Supporting Variants
SamplesHG01137
Known GenesAPTX
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13451450
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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