A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460230



Internal ID238221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163846001..163847827hg38UCSC Ensembl
chr4:164767153..164768979hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg381827
hg191827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16959807
Samples
Known GenesMARCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460230
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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