A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566096



Internal ID20939167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70953660..70954648hg38UCSC Ensembl
chr4:71819377..71820365hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38989
hg19989
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265986
Samples
Known GenesMOB1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566096
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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