A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624013



Internal ID21816060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2084989..2086605hg38UCSC Ensembl
chr19:2084988..2086604hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381617
hg191617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6041544
Supporting Variants
Samples
Known GenesMOB3A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624013
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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