A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573341



Internal ID20946412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92663836..92664842hg38UCSC Ensembl
chr7:92293150..92294156hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg381007
hg191007
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7011n223
Supporting Variantsnssv18276927
Samples
Known GenesCDK6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573341
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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