A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883359



Internal ID22658338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29175147..29175420hg38UCSC Ensembl
chr1:29501659..29501932hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352734
Samples
Known GenesSRSF4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883359
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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