A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275189



Internal ID20484407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64333733..64334063hg38UCSC Ensembl
chr4:65199451..65199781hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741805
Supporting Variants
Samples
Known GenesTECRL
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275189
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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