A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969880



Internal ID22744815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29665581..29665728hg38UCSC Ensembl
chr6:29633358..29633505hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445270
Samples
Known GenesMOG
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969880
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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