A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260448



Internal ID20469666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52796845..52797258hg38UCSC Ensembl
chr1:53262517..53262930hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748907
Supporting Variants
Samples
Known GenesZYG11B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260448
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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