A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460926



Internal ID22518809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70163013..70164812hg38UCSC Ensembl
chr10:71922769..71924568hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848100
Supporting Variants
Samples
Known GenesSAR1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460926
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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