A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408527



Internal ID22466397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41841395..41841543hg38UCSC Ensembl
chr19:42345490..42345638hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5930425
Supporting Variants
Samples
Known GenesLYPD4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408527
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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