A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653722



Internal ID21602027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100345064..100345064hg38UCSC Ensembl
chr14:100811401..100811401hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094282
SamplesHG00731
Known GenesWARS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653722
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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