A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566036



Internal ID20939107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82986353..82986478hg38UCSC Ensembl
chr4:83907506..83907631hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266573
Samples
Known GenesLIN54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566036
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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