A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566598



Internal ID20939669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142942863..142944078hg38UCSC Ensembl
chr4:143864016..143865231hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg381216
hg191216
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264745
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566598
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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