A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418694



Internal ID21076247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20241156..20247353hg38UCSC Ensembl
chr8:20098667..20104864hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg386198
hg196198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165408
Samples
Known GenesLZTS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418694
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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