A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829973



Internal ID22604908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28510701..28513950hg38UCSC Ensembl
chr1:28837213..28840462hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg383250
hg193250
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450825
Samples
Known GenesRCC1, SNHG3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829973
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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