A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574685



Internal ID20947756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:122936838..122938818hg38UCSC Ensembl
chr4:123857993..123859973hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg381981
hg191981
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263661
Samples
Known GenesSPATA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574685
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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