A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279069



Internal ID20488287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40358729..40358819hg38UCSC Ensembl
chr4:40360746..40360836hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748072
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279069
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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