A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738189



Internal ID20514156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207142884..207143206hg38UCSC Ensembl
chr1:207316229..207316551hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276428
Samples
Known GenesC4BPA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738189
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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