A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13529573



Internal ID6586529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76846032..76886813hg38UCSC Ensembl
chr9:79460948..79501729hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3840782
hg1940782
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620751
Supporting Variants
SamplesNA20766
Known GenesPRUNE2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13529573
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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