A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17390553



Internal ID22448423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3157250..3165421hg38UCSC Ensembl
chr19:3157248..3165419hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg388172
hg198172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935865
Supporting Variants
Samples
Known GenesGNA15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17390553
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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