A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13462127



Internal ID1221673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36458795..36466987hg38UCSC Ensembl
Innerchr9:36458795..36466987hg38UCSC Ensembl
Outerchr9:36458717..36467043hg38UCSC Ensembl
chr9:36458792..36466984hg19UCSC Ensembl
Innerchr9:36458792..36466984hg19UCSC Ensembl
Outerchr9:36458714..36467040hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg388193
hg198193
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620395
Supporting Variants
SamplesHG01085
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13462127
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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