A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554826



Internal ID20927916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9931562..9932582hg38UCSC Ensembl
chr1:9991620..9992640hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381021
hg191021
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252813
Samples
Known GenesLZIC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554826
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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