A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541851



Internal ID20915119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66558955..66559932hg38UCSC Ensembl
chr2:66786087..66787064hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38978
hg19978
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258819
Samples
Known GenesMEIS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541851
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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