A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401799



Internal ID21059352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154689900..154702328hg38UCSC Ensembl
chr5:154069460..154081888hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3812429
hg1912429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128748
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401799
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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