A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13436359



Internal ID6447976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28154618..28207642hg38UCSC Ensembl
chr9:28154616..28207640hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3853025
hg1953025
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620150
Supporting Variants
SamplesNA20511
Known GenesLINGO2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13436359
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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