A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881976



Internal ID22656953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57205576..57206638hg38UCSC Ensembl
chr19:57716944..57718006hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg381063
hg191063
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479296
Samples
Known GenesZNF264
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881976
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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