A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414098



Internal ID21071651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:105850543..105850991hg38UCSC Ensembl
chr5:105186244..105186692hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124016
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414098
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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