A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416524



Internal ID22474394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151316096..151317298hg38UCSC Ensembl
chr4:152237248..152238450hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg381203
hg191203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5890360
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416524
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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