A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829804



Internal ID22604739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25381354..25393334hg38UCSC Ensembl
chr1:25707845..25719825hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3811981
hg1911981
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450707, nssv17460188
Samples
Known GenesRHCE
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829804
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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