A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587580



Internal ID21779623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70845656..70845656hg38UCSC Ensembl
chr10:72605413..72605413hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091799
Supporting Variants
Samples
Known GenesSGPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587580
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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