A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17635092



Internal ID21827139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2433634..2433738hg38UCSC Ensembl
chr19:2433632..2433736hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6044674
Supporting Variants
Samples
Known GenesLMNB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17635092
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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