A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379577



Internal ID21037130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:28982701..29063900hg38UCSC Ensembl
chr5:28982808..29064007hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3881200
hg1981200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379577
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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