A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622050



Internal ID21814097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11556517..11556607hg38UCSC Ensembl
chr19:11667332..11667422hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6048734
Supporting Variants
Samples
Known GenesELOF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622050
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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