A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296489



Internal ID20505707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61571028..61571084hg38UCSC Ensembl
chr14:62037746..62037802hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740713
Supporting Variants
Samples
Known GenesFLJ22447
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296489
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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