A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818041



Internal ID21263379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142975358..142975739hg38UCSC Ensembl
chr8:144056775..144057156hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13696576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818041
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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