A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092809



Internal ID21431746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79187583..79187681hg38UCSC Ensembl
chr14:79653926..79654024hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597432
Supporting Variants
SamplesHG00731
Known GenesNRXN3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092809
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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