A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507480



Internal ID20880772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100198777..100209275hg38UCSC Ensembl
chr14:100665114..100675612hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3810499
hg1910499
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507480
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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