A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569009



Internal ID20942080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82985690..82986996hg38UCSC Ensembl
chr4:83906843..83908149hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg381307
hg191307
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266572
Samples
Known GenesLIN54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569009
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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