A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565158



Internal ID20938229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:137941977..138053563hg38UCSC Ensembl
chr4:138863131..138974717hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38111587
hg19111587
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263151
Samples
Known GenesLINC00616
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565158
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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