A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848436



Internal ID22623371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128219529..128230062hg38UCSC Ensembl
chr11:128089424..128099957hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3810534
hg1910534
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451380
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848436
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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