A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545346



Internal ID20918577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:231536912..231537741hg38UCSC Ensembl
chr1:231672658..231673487hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38830
hg19830
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250372
Samples
Known GenesTSNAX, TSNAX-DISC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545346
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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