A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829685



Internal ID22604620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29246816..29251206hg38UCSC Ensembl
chr1:29573328..29577718hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg384391
hg194391
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451815
Samples
Known GenesPTPRU
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829685
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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