A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13529574



Internal ID6586689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76849333..76868424hg38UCSC Ensembl
Innerchr9:76849333..76868424hg38UCSC Ensembl
Outerchr9:76848833..76868924hg38UCSC Ensembl
chr9:79464249..79483340hg19UCSC Ensembl
Innerchr9:79464249..79483340hg19UCSC Ensembl
Outerchr9:79463749..79483840hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3819092
hg1919092
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620752
Supporting Variants
SamplesNA20766
Known GenesPRUNE2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13529574
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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