A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958114



Internal ID39396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150161967..150172555hg38UCSC Ensembl
chr4:151083119..151093707hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3810589
hg1910589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459683
Supporting Variants
Samples
Known GenesDCLK2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958114
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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