A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545599



Internal ID20874095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207135065..207137632hg38UCSC Ensembl
chr1:207308410..207310977hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg382568
hg192568
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250011
Samples
Known GenesC4BPA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545599
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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