A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628218



Internal ID21820265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:723510..804661hg38UCSC Ensembl
chr19:723510..804661hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3881152
hg1981152
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6041107
Supporting Variants
Samples
Known GenesMISP, PALM, PTBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628218
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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