A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404600



Internal ID21062153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115067594..115069103hg38UCSC Ensembl
chr5:114403291..114404800hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg381510
hg191510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122836
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404600
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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