A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892913



Internal ID22667969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38176831..38178476hg38UCSC Ensembl
chr4:38178452..38180097hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381646
hg191646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426221
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892913
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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