A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454978



Internal ID22512855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:107370569..107378840hg38UCSC Ensembl
chr10:109130327..109138598hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg388272
hg198272
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848999
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454978
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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