A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630826



Internal ID21822873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9845269..9845390hg38UCSC Ensembl
chr19:9955945..9956066hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046349
Supporting Variants
Samples
Known GenesPIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630826
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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