A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884143



Internal ID22659125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14584580..14589613hg38UCSC Ensembl
chr19:14695392..14700425hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg385034
hg195034
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473231, nssv17473230
Samples
Known GenesCLEC17A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884143
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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