A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750058



Internal ID20526093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112988860..112988970hg38UCSC Ensembl
chr13:113643174..113643284hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292177
Samples
Known GenesMCF2L
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750058
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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