A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036569



Internal ID21945912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24193768..24193843hg38UCSC Ensembl
chr14:24662974..24663049hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615506
Samples
Known GenesTM9SF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036569
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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