A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17562186



Internal ID21886541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99053600..99053600hg38UCSC Ensembl
chr7:98651223..98651223hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6075077
Supporting Variants
Samples
Known GenesSMURF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17562186
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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