A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13569805



Internal ID3080485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94474648..94488233hg38UCSC Ensembl
Innerchr9:94474680..94488202hg38UCSC Ensembl
Outerchr9:94474617..94488265hg38UCSC Ensembl
chr9:97236930..97250515hg19UCSC Ensembl
Innerchr9:97236962..97250484hg19UCSC Ensembl
Outerchr9:97236899..97250547hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3813586
hg1913586
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621124
Supporting Variants
SamplesHG02702
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13569805
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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