A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464293



Internal ID22522179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11773221..11775396hg38UCSC Ensembl
chr10:11815220..11817395hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382176
hg192176
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856204
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464293
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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