A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17496209



Internal ID22554142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:144516936..144520142hg38UCSC Ensembl
chr5:143896499..143899705hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg383207
hg193207
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841795
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17496209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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