A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602878



Internal ID21551538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96364894..96366309hg38UCSC Ensembl
chr14:96831231..96832646hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381416
hg191416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087299
SamplesNA19983
Known GenesGSKIP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602878
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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