A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449218



Internal ID22507088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116254679..116258552hg38UCSC Ensembl
chr9:119016958..119020831hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg383874
hg193874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908953
Supporting Variants
Samples
Known GenesPAPPA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449218
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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