A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088573



Internal ID21509031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90621224..90621334hg38UCSC Ensembl
chr14:91087568..91087678hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584605
Supporting Variants
SamplesNA20847
Known GenesTTC7B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088573
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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