A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497256



Internal ID22555190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77570710..77576213hg38UCSC Ensembl
chr4:78491864..78497367hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg385504
hg195504
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840393
Supporting Variants
Samples
Known GenesCXCL13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497256
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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