A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413611



Internal ID21071164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113742875..113854223hg38UCSC Ensembl
chr5:113078572..113189920hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38111349
hg19111349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123161
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413611
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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