A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871299



Internal ID22646236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37962189..37964688hg38UCSC Ensembl
chr19:38452829..38455328hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475349
Samples
Known GenesSIPA1L3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871299
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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