A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17390806



Internal ID22448676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40355389..40358342hg38UCSC Ensembl
chr19:40861296..40864249hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382954
hg192954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934074
Supporting Variants
Samples
Known GenesPLD3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17390806
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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