A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276349



Internal ID20485567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161923727..161923789hg38UCSC Ensembl
chr1:161893517..161893579hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742585
Supporting Variants
Samples
Known GenesATF6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276349
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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