A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540685



Internal ID20913974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224444650..224445547hg38UCSC Ensembl
chr1:224632352..224633249hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg38898
hg19898
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249381
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540685
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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