A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624250



Internal ID21816297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55147714..55147791hg38UCSC Ensembl
chr19:55659082..55659159hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6059742
Supporting Variants
Samples
Known GenesTNNT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624250
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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