A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497254



Internal ID22555188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77514760..77517992hg38UCSC Ensembl
chr4:78435914..78439146hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg383233
hg193233
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840118
Supporting Variants
Samples
Known GenesCXCL13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497254
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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