A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498903



Internal ID22556838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:128609656..128613084hg38UCSC Ensembl
chr4:129530811..129534239hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg383429
hg193429
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837934
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498903
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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