A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565399



Internal ID20938470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82508487..82509790hg38UCSC Ensembl
chr4:83429640..83430943hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg381304
hg191304
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266451
Samples
Known GenesTMEM150C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565399
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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