A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2799618



Internal ID21244956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58600127..58600219hg38UCSC Ensembl
chr19:59111494..59111586hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13681154
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2799618
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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