A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466386



Internal ID244227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163668077..163668154hg38UCSC Ensembl
chr4:164589229..164589306hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16959786
Samples
Known GenesMARCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466386
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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