A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601754



Internal ID21793801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101261255..101261947hg38UCSC Ensembl
chr14:101727592..101728284hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38693
hg19693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027396
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601754
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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