A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459127



Internal ID22517009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62738993..62743717hg38UCSC Ensembl
chr10:64498753..64503477hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg384725
hg194725
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854217
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459127
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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