A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397755



Internal ID22455625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44922115..44933226hg38UCSC Ensembl
chr19:45425372..45436483hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3811112
hg1911112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944738
Supporting Variants
Samples
Known GenesAPOC1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397755
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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