A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474885



Internal ID22532780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89989623..89992720hg38UCSC Ensembl
chr15:90532855..90535952hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383098
hg193098
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876058
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474885
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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