A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887941



Internal ID22662940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14341178..14348574hg38UCSC Ensembl
chr4:14342802..14350198hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg387397
hg197397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411901
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887941
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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