A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16950998



Internal ID34695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52794123..52794555hg38UCSC Ensembl
chr4:53660290..53660722hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454526
Supporting Variants
Samples
Known GenesLOC152578
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16950998
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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