A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829036



Internal ID22603971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:192877458..192879057hg38UCSC Ensembl
chr1:192846588..192848187hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462318, nssv17454468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829036
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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