A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467192



Internal ID245011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76709018..76726256hg38UCSC Ensembl
chr4:77630171..77647409hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3817239
hg1917239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16952367
Samples
Known GenesSHROOM3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467192
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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