A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883926



Internal ID22658908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27748333..27748534hg38UCSC Ensembl
chr1:28074844..28075045hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357676
Samples
Known GenesFAM76A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883926
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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