A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399247



Internal ID21056800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164943320..165095952hg38UCSC Ensembl
chr5:164370326..164522958hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38152633
hg19152633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128257
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399247
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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