A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537842



Internal ID20911174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:171336346..171338566hg38UCSC Ensembl
chr2:172192856..172195076hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg382221
hg192221
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256054
Samples
Known GenesMETTL8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537842
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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