A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664443



Internal ID21612748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96415728..96415728hg38UCSC Ensembl
chr14:96882065..96882065hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098798
SamplesNA19238
Known GenesAK7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664443
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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