A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639584



Internal ID6679675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89504768..89531669hg38UCSC Ensembl
Innerchr16:89505268..89531169hg38UCSC Ensembl
Outerchr16:89503768..89532669hg38UCSC Ensembl
chr16:89571176..89598077hg19UCSC Ensembl
Innerchr16:89571676..89597577hg19UCSC Ensembl
Outerchr16:89570176..89599077hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3826902
hg1926902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15569836
SamplesHG02128
Known GenesSPG7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639584
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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