A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572993



Internal ID20946064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82487177..82488871hg38UCSC Ensembl
chr4:83408330..83410024hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg381695
hg191695
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266449
Samples
Known GenesTMEM150C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572993
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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