A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399576



Internal ID21057129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:105826069..105915444hg38UCSC Ensembl
chr5:105161770..105251145hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3889376
hg1989376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124011
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399576
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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