A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465667



Internal ID22523556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103355875..103367091hg38UCSC Ensembl
chr10:105115632..105126848hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3811217
hg1911217
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860008
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465667
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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