A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17491960



Internal ID22549887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186616957..186620306hg38UCSC Ensembl
chr4:187538111..187541460hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg383350
hg193350
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838513
Supporting Variants
Samples
Known GenesFAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17491960
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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