A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456419



Internal ID234487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:92051625..92545686hg38UCSC Ensembl
chr4:92972776..93466837hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38494062
hg19494062
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16953840
Samples
Known GenesGRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456419
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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