A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818940



Internal ID21264279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58165895..58166230hg38UCSC Ensembl
chr8:59078454..59078789hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13707546
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818940
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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