A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5648676



Internal ID21596981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91412198..91412198hg38UCSC Ensembl
chr14:91878542..91878542hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17083906
SamplesHG03125
Known GenesCCDC88C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5648676
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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