A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286918



Internal ID20496136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99410397..99410397hg38UCSC Ensembl
chr7:99008020..99008020hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763138
Supporting Variants
Samples
Known GenesBUD31
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286918
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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