A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325991



Internal ID20859125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109811190..109813998hg38UCSC Ensembl
chr1:110353812..110356620hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg382809
hg192809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050829
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325991
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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