A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17499377



Internal ID22557312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108997519..109012702hg38UCSC Ensembl
chr5:108333220..108348403hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3815184
hg1915184
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840887
Supporting Variants
Samples
Known GenesFER
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17499377
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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