A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291014



Internal ID20500232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155733467..155733467hg38UCSC Ensembl
chr7:155526161..155526161hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753387
Supporting Variants
Samples
Known GenesRBM33
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291014
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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