A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361152



Internal ID22586821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61225600..61238780hg38UCSC Ensembl
chr10:62985358..62998538hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3813181
hg1913181
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927382
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361152
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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