A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286006



Internal ID20495224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44042394..44042394hg38UCSC Ensembl
chr6:44010131..44010131hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752701
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286006
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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