A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17476697



Internal ID22534595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43476621..43477840hg38UCSC Ensembl
chr19:43980773..43981992hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg381220
hg191220
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874458
Supporting Variants
Samples
Known GenesPHLDB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17476697
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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