A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492864



Internal ID22550792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:133121954..133126053hg38UCSC Ensembl
chr4:134043109..134047208hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837365
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492864
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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