A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562120



Internal ID335079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148789800..148789898hg38UCSC Ensembl
chr6:149110936..149111034hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16988944
Samples
Known GenesUST
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562120
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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