A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457360



Internal ID22515241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16412134..16419711hg38UCSC Ensembl
chr10:16454133..16461710hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg387578
hg197578
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5847818
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457360
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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