A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829380



Internal ID22604315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225420051..225421234hg38UCSC Ensembl
chr1:225607753..225608936hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg381184
hg191184
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466132
Samples
Known GenesLBR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829380
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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