A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588269



Internal ID21780312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73429776..73429776hg38UCSC Ensembl
chr10:75189534..75189534hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094597
Supporting Variants
Samples
Known GenesMSS51
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588269
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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