A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860596



Internal ID22635531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95261480..95263725hg38UCSC Ensembl
chr11:94994644..94996889hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg382246
hg192246
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467999
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860596
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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