A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275393



Internal ID20484611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20405907..20406897hg38UCSC Ensembl
chr4:20407530..20408520hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38991
hg19991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732522
Supporting Variants
Samples
Known GenesSLIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275393
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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