A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610173



Internal ID21802220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36531288..36531342hg38UCSC Ensembl
chr14:37000493..37000547hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032975
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610173
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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