A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492798



Internal ID22550726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20433973..20437397hg38UCSC Ensembl
chr4:20435596..20439020hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg383425
hg193425
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838633
Supporting Variants
Samples
Known GenesSLIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492798
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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