A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520690



Internal ID21845049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:121830174..121830709hg38UCSC Ensembl
chr1:121360712..121361247hg19UCSC Ensembl
Cytoband1p11.2
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5980966
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520690
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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