A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454802



Internal ID22512679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69651937..69661879hg38UCSC Ensembl
chr10:71411693..71421635hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg389943
hg199943
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850126
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454802
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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