A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540845



Internal ID20914133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:109263059..109263741hg38UCSC Ensembl
chr2:109879515..109880197hg19UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg38683
hg19683
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256467
Samples
Known GenesSH3RF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540845
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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