A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17572947



Internal ID21764990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:30987246..30987337hg38UCSC Ensembl
chr6:30955023..30955114hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008260
Supporting Variants
Samples
Known GenesMUC21
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17572947
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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