A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16954414



Internal ID36935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:104625447..105196966hg38UCSC Ensembl
chr4:105546604..106118123hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38571520
hg19571520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458684
Supporting Variants
Samples
Known GenesTET2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16954414
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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