A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462120



Internal ID22520005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69471181..69478281hg38UCSC Ensembl
chr10:71230937..71238037hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg387101
hg197101
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863290
Supporting Variants
Samples
Known GenesTSPAN15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462120
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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