A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828100



Internal ID22603035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145603079..145622816hg38UCSC Ensembl
chr1:145812240..145831984hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg3819738
hg1919745
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456132, nssv17467547
Samples
Known GenesGPR89A, LOC100288142, LOC101929780, NBPF10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828100
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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