A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16956050



Internal ID38005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:113233105..113233433hg38UCSC Ensembl
chr4:114154261..114154589hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459246
Supporting Variants
Samples
Known GenesANK2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16956050
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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