A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897197



Internal ID22672296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41225545..41230222hg38UCSC Ensembl
chr4:41227562..41232239hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg384678
hg194678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424187
Samples
Known GenesUCHL1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897197
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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