A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870947



Internal ID22645884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2820679..2821778hg38UCSC Ensembl
chr19:2820677..2821776hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474628
Samples
Known GenesZNF554
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870947
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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