A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848629



Internal ID22623564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60752603..60754602hg38UCSC Ensembl
chr11:60520076..60522075hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848629
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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