A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092122



Internal ID21431998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77269715..77269800hg38UCSC Ensembl
chr14:77736058..77736143hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585650
Supporting Variants
SamplesHG00731
Known GenesNGB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092122
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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