A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13538748



Internal ID1965764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81952502..81975850hg38UCSC Ensembl
Innerchr9:81952502..81975850hg38UCSC Ensembl
Outerchr9:81952002..81976350hg38UCSC Ensembl
chr9:84567417..84590765hg19UCSC Ensembl
Innerchr9:84567417..84590765hg19UCSC Ensembl
Outerchr9:84566917..84591265hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3823349
hg1923349
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620879
Supporting Variants
SamplesHG01815
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13538748
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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