A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951002



Internal ID34698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52853615..52866907hg38UCSC Ensembl
chr4:53719782..53733074hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3813293
hg1913293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460262
Supporting Variants
Samples
Known GenesRASL11B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951002
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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