A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878623



Internal ID22653589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2900693..2909192hg38UCSC Ensembl
chr19:2900691..2909190hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474636
Samples
Known GenesZNF57
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878623
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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