A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15569837



Internal ID5571653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89514722..89527655hg38UCSC Ensembl
chr16:89581130..89594063hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3812934
hg1912934
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639585
Supporting Variants
SamplesHG02128
Known GenesSPG7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15569837
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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