A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445798



Internal ID21103351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30596728..30611959hg38UCSC Ensembl
chr10:30885657..30900888hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3815232
hg1915232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981408
Samples
Known GenesLYZL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445798
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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