A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886174



Internal ID22661160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12544974..12549798hg38UCSC Ensembl
chr19:12655788..12660612hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384825
hg194825
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479960
Samples
Known GenesZNF564
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886174
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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