A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469971



Internal ID22527861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100352626..100361550hg38UCSC Ensembl
chr15:100892831..100901755hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg388925
hg198925
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5883305
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469971
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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