A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17521000



Internal ID21845359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211849012..211853922hg38UCSC Ensembl
chr1:212022354..212027264hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg384911
hg194911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982313
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17521000
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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