A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745736



Internal ID20521746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91105398..91106120hg38UCSC Ensembl
chr14:91571742..91572464hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38723
hg19723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272892
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745736
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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