A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600007



Internal ID21792054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31437032..31437351hg38UCSC Ensembl
chr14:31906238..31906557hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023725
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600007
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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