A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16953256



Internal ID36190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99923213..99924622hg38UCSC Ensembl
chr4:100844370..100845779hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg381410
hg191410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472575
Supporting Variants
Samples
Known GenesDNAJB14
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16953256
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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