A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828097



Internal ID22603032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145548167..145564558hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3816392
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456963, nssv17458383
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828097
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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