A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855276



Internal ID22630211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85654999..85657848hg38UCSC Ensembl
chr11:85366043..85368892hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg382850
hg192850
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450802
Samples
Known GenesCREBZF, TMEM126A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855276
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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