A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583053



Internal ID21775096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59696984..59697115hg38UCSC Ensembl
chr10:61456742..61456873hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6018301
Supporting Variants
Samples
Known GenesSLC16A9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583053
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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