A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543662



Internal ID20916908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150492701..150493183hg38UCSC Ensembl
chr1:150465177..150465659hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247528
Samples
Known GenesTARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543662
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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