A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488509



Internal ID21146062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70854729..70865916hg38UCSC Ensembl
chr14:71321446..71332633hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3811188
hg1911188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021270
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488509
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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