A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084344



Internal ID21447441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76496401..76496401hg38UCSC Ensembl
chr14:76962744..76962744hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644770
Supporting Variants
SamplesHG00732
Known GenesESRRB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084344
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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