A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039662



Internal ID21949005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69820560..69831364hg38UCSC Ensembl
chr14:70287277..70298081hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3810805
hg1910805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039662
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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