A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972142



Internal ID22747077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3140044..3140044hg38UCSC Ensembl
chr19:3140042..3140042hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394602
Samples
Known GenesGNA15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972142
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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