A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406006



Internal ID22463876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31199764..31199764hg38UCSC Ensembl
chr19:31690670..31690670hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38497
hg19497
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976384
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406006
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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