A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16967700



Internal ID45777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43195429..43196366hg38UCSC Ensembl
chr5:43195531..43196468hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38938
hg19938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470167
Supporting Variants
Samples
Known GenesNIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16967700
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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