A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898501



Internal ID22673617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18894642..18894697hg38UCSC Ensembl
chr4:18896265..18896320hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427598
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898501
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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