A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080716



Internal ID21461316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76476689..76476738hg38UCSC Ensembl
chr14:76943032..76943081hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586456
Supporting Variants
SamplesHG02818
Known GenesESRRB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080716
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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