A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16953484



Internal ID36341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103061273..103062279hg38UCSC Ensembl
chr4:103982430..103983436hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg381007
hg191007
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457854
Supporting Variants
Samples
Known GenesSLC9B2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16953484
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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