A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602978



Internal ID21551639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:33223816..33224557hg38UCSC Ensembl
chr14:33693022..33693763hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081601
SamplesHG02492
Known GenesNPAS3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602978
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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