A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377229



Internal ID21034782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8212831..8222354hg38UCSC Ensembl
chr5:8212944..8222467hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg389524
hg199524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132957
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377229
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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