A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13511443



Internal ID3513259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69474028..69502727hg38UCSC Ensembl
chr9:72088944..72117643hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3828700
hg1928700
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620560
Supporting Variants
SamplesHG02805
Known GenesAPBA1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13511443
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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