A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18122289



Internal ID20689329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10501225..10502127hg38UCSC Ensembl
chr5:10501337..10502239hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38903
hg19903
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381140
Supporting Variants
Samples
Known GenesLOC101929412
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18122289
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00014


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