A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579964



Internal ID20953035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51824223..51825238hg38UCSC Ensembl
chr14:52290941..52291956hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg381016
hg191016
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221916
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579964
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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