A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574704



Internal ID20947775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131268599..131270004hg38UCSC Ensembl
chr5:130604292..130605697hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg381406
hg191406
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5935n223
Supporting Variantsnssv18267896
Samples
Known GenesCDC42SE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574704
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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