A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462890



Internal ID240812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107867723..107869708hg38UCSC Ensembl
chr4:108788879..108790864hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381986
hg191986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16954830
Samples
Known GenesSGMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462890
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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