A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275726



Internal ID20484944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156695271..156695343hg38UCSC Ensembl
chr1:156665063..156665135hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734341
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275726
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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