A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888329



Internal ID22663333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43985513..43985571hg38UCSC Ensembl
chr4:43987530..43987588hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422470
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888329
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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