A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542926



Internal ID20916177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235665110..235665316hg38UCSC Ensembl
chr1:235828410..235828616hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250727
Samples
Known GenesLYST
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542926
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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