A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292201



Internal ID20501419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183614132..183614255hg38UCSC Ensembl
chr1:183583267..183583390hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737446
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292201
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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