A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459663



Internal ID22517549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18183656..18190935hg38UCSC Ensembl
chrUn_gl000212:12408..19687hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg387280
hg197280
Variant TypeOTHER copy number variation
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863518
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459663
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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