A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492262



Internal ID22550189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:114879973..114938137hg38UCSC Ensembl
chr4:115801129..115859293hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3858165
hg1958165
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836979
Supporting Variants
Samples
Known GenesNDST4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492262
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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