A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036152



Internal ID21945495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87015401..87021948hg38UCSC Ensembl
chr14:87481745..87488292hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg386548
hg196548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611570
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036152
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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