A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2798483



Internal ID21243821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58460109..58460178hg38UCSC Ensembl
chr18:56127341..56127410hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13707491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2798483
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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