A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870288



Internal ID22645224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19011197..19012246hg38UCSC Ensembl
chr19:19122006..19123055hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381050
hg191050
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473866
Samples
Known GenesSUGP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870288
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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