A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13451396



Internal ID5774027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32716372..32735734hg38UCSC Ensembl
chr9:32716370..32735732hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3819363
hg1919363
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620309
Supporting Variants
SamplesNA19143
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13451396
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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