A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922500



Internal ID22697725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85635778..85636044hg38UCSC Ensembl
chr11:85346822..85347088hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354154
Samples
Known GenesTMEM126B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922500
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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