A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738150



Internal ID20514117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34443194..34443362hg38UCSC Ensembl
chr14:34912400..34912568hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268607
Samples
Known GenesSPTSSA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738150
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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