A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355951



Internal ID22581620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21484540..21489203hg38UCSC Ensembl
chr10:21773469..21778132hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg384664
hg194664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925993
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355951
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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