A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901642



Internal ID22676794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151917837..151917897hg38UCSC Ensembl
chr4:152838989..152839049hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425553
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901642
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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