A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13619357



Internal ID951349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126145176..126149863hg38UCSC Ensembl
Innerchr9:126145176..126149863hg38UCSC Ensembl
Outerchr9:126144913..126150090hg38UCSC Ensembl
chr9:128907455..128912142hg19UCSC Ensembl
Innerchr9:128907455..128912142hg19UCSC Ensembl
Outerchr9:128907192..128912369hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg384688
hg194688
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621760
Supporting Variants
SamplesHG00583
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13619357
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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