A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16956615



Internal ID38384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146554702..146572155hg38UCSC Ensembl
chr4:147475854..147493307hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3817454
hg1917454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460791
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16956615
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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