A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746177



Internal ID20522188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22891370..22891448hg38UCSC Ensembl
chr14:23360579..23360657hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260683
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746177
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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