A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873940



Internal ID22648890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13815636..13817041hg38UCSC Ensembl
chr19:13926450..13927855hg19UCSC Ensembl
Cytoband19p13.13
Allele length
AssemblyAllele length
hg381406
hg191406
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473212
Samples
Known GenesZSWIM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873940
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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