A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511882



Internal ID20885212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100756555..100758906hg38UCSC Ensembl
chr14:101222892..101225243hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg382352
hg192352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511882
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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