A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17496353



Internal ID22554287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155125649..155144703hg38UCSC Ensembl
chr5:154505209..154524263hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3819055
hg1919055
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841204
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17496353
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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