A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893011



Internal ID22668068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121238688..121238764hg38UCSC Ensembl
chr4:122159843..122159919hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410110
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893011
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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