A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594826



Internal ID20967897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:47163920..47164852hg38UCSC Ensembl
chr17:45241286..45242218hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38933
hg19933
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3177n223
Supporting Variantsnssv18242466
Samples
Known GenesCDC27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594826
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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