A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882612



Internal ID22657589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19693107..19697697hg38UCSC Ensembl
chr19:19803916..19808506hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg384591
hg194591
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473880
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882612
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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