A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671646



Internal ID21619951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:120133330..120151475hg38UCSC Ensembl
chr1:120675901..120694037hg19UCSC Ensembl
Cytoband1p11.2
Allele length
AssemblyAllele length
hg3818146
hg1918137
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17060184
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671646
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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