A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263669



Internal ID20472887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6300699..6300699hg38UCSC Ensembl
chr1:6360759..6360759hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762676
Supporting Variants
Samples
Known GenesACOT7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263669
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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