A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877220



Internal ID22652183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153032465..153032536hg38UCSC Ensembl
chr1:153004941..153005012hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359889
Samples
Known GenesSPRR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877220
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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