A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730664



Internal ID20506576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169850984..169851061hg38UCSC Ensembl
chr1:169820125..169820202hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281331
Samples
Known GenesC1orf112
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730664
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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