A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545169



Internal ID20918401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:200961664..200961765hg38UCSC Ensembl
chr1:200930792..200930893hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248299
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545169
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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