A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900541



Internal ID22675684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154523603..154523814hg38UCSC Ensembl
chr4:155444755..155444966hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900541
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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