A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546382



Internal ID20919600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150135701..150136041hg38UCSC Ensembl
chr1:150107862..150108202hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247511
Samples
Known GenesVPS45
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546382
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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