A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890071



Internal ID22665096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17613295..17613637hg38UCSC Ensembl
chr4:17614918..17615260hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412743
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890071
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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