A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17529399



Internal ID21853756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47337075..47337156hg38UCSC Ensembl
chr1:47802747..47802828hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984593
Supporting Variants
Samples
Known GenesCMPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17529399
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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