A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475976



Internal ID22533874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42530643..42533565hg38UCSC Ensembl
chr19:43034795..43037717hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382923
hg192923
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873458
Supporting Variants
Samples
Known GenesLIPE-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475976
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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