A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574151



Internal ID20947222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148220176..148220598hg38UCSC Ensembl
chr4:149141327..149141749hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264830
Samples
Known GenesNR3C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574151
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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