A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16952101



Internal ID35425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70995524..70995805hg38UCSC Ensembl
chr4:71861241..71861522hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470283
Supporting Variants
Samples
Known GenesDCK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16952101
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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