A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560037



Internal ID20933108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140885477..140886013hg38UCSC Ensembl
chr4:141806631..141807167hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264730
Samples
Known GenesRNF150
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560037
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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