A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976105



Internal ID22751040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170264882..170388789hg38UCSC Ensembl
chr6:170573970..170697877hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38123908
hg19123908
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426915
Samples
Known GenesDLL1, FAM120B, FLJ38122, MIR4644
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976105
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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