A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287641



Internal ID20496859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23232826..23232902hg38UCSC Ensembl
chr14:23702035..23702111hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736776
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287641
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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