A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17378736



Internal ID22436606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27547752..27549207hg38UCSC Ensembl
chr15:27792898..27794353hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381456
hg191456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932673
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17378736
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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