A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556303



Internal ID20929374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140104220..140104678hg38UCSC Ensembl
chr4:141025374..141025832hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264719
Samples
Known GenesMAML3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556303
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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