A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881490



Internal ID22656466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15785108..15786950hg38UCSC Ensembl
chr1:16111603..16113445hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg381843
hg191843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356206
Samples
Known GenesFBLIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881490
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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