A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577762



Internal ID20950833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71767566..71767652hg38UCSC Ensembl
chr14:72234283..72234369hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238613
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577762
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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