A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450352



Internal ID22508222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87561873..87584245hg38UCSC Ensembl
chr10:89321630..89344002hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3822373
hg1922373
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852890
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450352
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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