A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537365



Internal ID20910703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101049462..101050118hg38UCSC Ensembl
chr2:101665924..101666580hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38657
hg19657
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255723
Samples
Known GenesTBC1D8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537365
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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