A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471799



Internal ID22529691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38751320..38766630hg38UCSC Ensembl
chr15:39043521..39058831hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3815311
hg1915311
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865681
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471799
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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