A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554741



Internal ID20927832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:213225583..213226191hg38UCSC Ensembl
chr1:213398926..213399534hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248544
Samples
Known GenesRPS6KC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554741
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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