A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548470



Internal ID20921656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168188866..168188984hg38UCSC Ensembl
chr1:168158104..168158222hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248049
Samples
Known GenesTIPRL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548470
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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