A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585412



Internal ID21533959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61571027..61571083hg38UCSC Ensembl
chr14:62037745..62037801hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096566
SamplesNA18939
Known GenesFLJ22447
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585412
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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