A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098500



Internal ID21456260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58828105..58828105hg38UCSC Ensembl
chr14:59294823..59294823hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650694
Supporting Variants
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098500
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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