A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623258



Internal ID21815305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55434309..55434376hg38UCSC Ensembl
chr19:55945676..55945743hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6047667
Supporting Variants
Samples
Known GenesSHISA7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623258
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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