A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672101



Internal ID21620406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26979174..27025303hg38UCSC Ensembl
chr15:27224321..27270450hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3846130
hg1946130
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095228
SamplesHG02492
Known GenesGABRG3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672101
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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