A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904871



Internal ID22680050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:28853550..28857714hg38UCSC Ensembl
chr5:28853657..28857821hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg384165
hg194165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415283
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904871
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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