A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554037



Internal ID20927146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:213092631..213093007hg38UCSC Ensembl
chr1:213265973..213266349hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248540
Samples
Known GenesRPS6KC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554037
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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