A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453132



Internal ID22511005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100594640..100602189hg38UCSC Ensembl
chr10:102354397..102361946hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg387550
hg197550
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852611
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453132
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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