A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557686



Internal ID330777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1303350..1304488hg38UCSC Ensembl
chr6:1303585..1304723hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381139
hg191139
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977823
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557686
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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