A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875113



Internal ID22650068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20944982..20946481hg38UCSC Ensembl
chr19:21127788..21129287hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473958, nssv17473959
Samples
Known GenesZNF85
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875113
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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