A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16954109



Internal ID36734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118901914..118902033hg38UCSC Ensembl
chr4:119823069..119823188hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467399
Supporting Variants
Samples
Known GenesSYNPO2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16954109
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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