A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094664



Internal ID21431221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102379630..102379680hg38UCSC Ensembl
chr14:102845967..102846017hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600282
Supporting Variants
SamplesHG00731
Known GenesTECPR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094664
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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